{"id":51129,"date":"2024-10-14T17:06:05","date_gmt":"2024-10-14T09:06:05","guid":{"rendered":"http:\/\/www.newtopchem.com\/archives\/51129"},"modified":"2024-10-14T17:06:05","modified_gmt":"2024-10-14T09:06:05","slug":"study-on-the-catalytic-effect-and-selectivity-of-cyclohexylamine-in-organic-synthesis-reactions","status":"publish","type":"post","link":"http:\/\/www.newtopchem.com\/archives\/51129","title":{"rendered":"Study on the catalytic effect and selectivity of cyclohexylamine in organic synthesis reactions","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"<h3 data-spm-anchor-id=\"5176.28103460.0.i16.45ea5d27JUwM1I\">Study on the catalytic effect and selectivity of cyclohexylamine in organic synthesis reactions<\/h3>\n<h4>Abstract<\/h4>\n<p>Cyclohexylamine (CHA), as a common organic compound, has important application value in the field of organic synthesis.  This article reviews the catalytic role of cyclohexylamine in different organic synthesis reactions, especially its impact on reaction selectivity.  Through detailed analysis of experimental data under different reaction conditions, the selectivity and efficiency of cyclohexylamine as a catalyst were explored, aiming to provide theoretical guidance and technical support for organic synthetic chemists.  <\/p>\n<h4>1. Introduction<\/h4>\n<p>Cyclohexylamine (CHA) is a colorless liquid with strong alkalinity and certain nucleophilicity. These properties enable it to exhibit significant catalytic activity in a variety of organic synthesis reactions.  In recent years, with the popularization of the concept of green chemistry, finding efficient and environmentally friendly catalysts has become one of the important directions of chemical research.  Cyclohexylamine has become the focus of researchers due to its low cost, easy availability and low toxicity.  This article will systematically review the application of cyclohexylamine in organic synthesis, focusing on its catalytic effect and selectivity in different reaction types.  <\/p>\n<h4>2. Physical and chemical properties of cyclohexylamine<\/h4>\n<ul>\n<li><strong>Molecular formula<\/strong>: C6H11NH2<\/li>\n<li><strong>Molecular weight<\/strong>: 99.16 g\/mol<\/li>\n<li><strong>Boiling point<\/strong>: 135.7\u00b0C<\/li>\n<li><strong>Melting point<\/strong>: -18.2\u00b0C<\/li>\n<li><strong>Solubility<\/strong>: Soluble in most organic solvents such as water and ethanol<\/li>\n<li><strong>Alkaline<\/strong>: Cyclohexylamine is highly alkaline, with a pKa value of approximately 11.3<\/li>\n<li><strong>Nucleophilicity<\/strong>: Cyclohexylamine has a certain nucleophilicity and can react with a variety of electrophiles<\/li>\n<\/ul>\n<h4>3. Catalytic application of cyclohexylamine in organic synthesis<\/h4>\n<h5>3.1 Acylation reaction<\/h5>\n<p>Cyclohexylamine exhibits excellent catalytic properties in acylation reactions, especially in esterification reactions.  Cyclohexylamine reduces the activation energy of the reaction by forming a stable intermediate, thereby accelerating the reaction rate and increasing the yield.  <\/p>\n<p><strong>3.1.1 Esterification reaction of carboxylic acid and alcohol<\/strong><\/p>\n<p>Table 1 shows the effect of cyclohexylamine on the esterification reaction of carboxylic acid and alcohol under different conditions.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Reaction conditions<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Reaction time (h)<\/th>\n<th>Yield (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>No catalyst<\/td>\n<td>\u2013<\/td>\n<td>24<\/td>\n<td>45<\/td>\n<\/tr>\n<tr>\n<td>Cyclohexylamine<\/td>\n<td>5<\/td>\n<td>12<\/td>\n<td>80<\/td>\n<\/tr>\n<tr>\n<td>Cyclohexylamine<\/td>\n<td>10<\/td>\n<td>8<\/td>\n<td>85<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>3.1.2 Esterification reaction of acid chloride and alcohol<\/strong><\/p>\n<p>Cyclohexylamine also shows good catalytic effect in the esterification reaction of acid chlorides and alcohols.  Table 2 lists several typical cases.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Acid chloride<\/th>\n<th>Alcohol<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Acetyl chloride<\/td>\n<td>Ethanol<\/td>\n<td>5<\/td>\n<td>90<\/td>\n<\/tr>\n<tr>\n<td>Propionyl chloride<\/td>\n<td>Ethanol<\/td>\n<td>5<\/td>\n<td>88<\/td>\n<\/tr>\n<tr>\n<td>Butyryl chloride<\/td>\n<td>Ethanol<\/td>\n<td>5<\/td>\n<td>85<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h5>3.2 Addition reaction<\/h5>\n<p>Cyclohexylamine also shows significant catalytic activity in addition reactions, especially in the reactions of aldehydes, ketones and nucleophiles.  <\/p>\n<p><strong>3.2.1 Addition reaction of aldehydes and nucleophiles<\/strong><\/p>\n<p>Table 3 shows the effect of cyclohexylamine on the addition reaction of aldehydes and nucleophiles.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Aldehyde<\/th>\n<th>Nucleophile<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Benzaldehyde<\/td>\n<td>Sodium methoxide<\/td>\n<td>5<\/td>\n<td>75<\/td>\n<\/tr>\n<tr>\n<td>Formaldehyde<\/td>\n<td>Sodium ethylate<\/td>\n<td>5<\/td>\n<td>80<\/td>\n<\/tr>\n<tr>\n<td>Propanal<\/td>\n<td>Sodium ethylate<\/td>\n<td>5<\/td>\n<td>78<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>3.2.2 Addition reaction of ketones and nucleophiles<\/strong><\/p>\n<p>Cyclohexylamine also shows good catalytic effect in the addition reaction of ketones and nucleophiles.  Table 4 lists several typical cases.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Keto<\/th>\n<th>Nucleophile<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Acetone<\/td>\n<td>Sodium ethylate<\/td>\n<td>3<\/td>\n<td>82<\/td>\n<\/tr>\n<tr>\n<td>Cyclohexanone<\/td>\n<td>Sodium ethylate<\/td>\n<td>4<\/td>\n<td>88<\/td>\n<\/tr>\n<tr>\n<td>Methyl Ketone<\/td>\n<td>Sodium ethylate<\/td>\n<td>3<\/td>\n<td>80<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h5>3.3 Reduction reaction<\/h5>\n<p>Cyclohexylamine can also serve as a cocatalyst in reduction reactions, especially when using metal hydrides such as sodium borohydride or lithium aluminum hydride.  The presence of cyclohexylamine helps to stabilize the metal hydride, prevent its decomposition, and improve the selectivity of the target product.  <\/p>\n<p><strong>3.3.1 Sodium borohydride reduction reaction<\/strong><\/p>\n<p>Table 5 shows the effect of cyclohexylamine on the reduction reaction of sodium borohydride.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Substrate<\/th>\n<th>Reducing agent<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Acetone<\/td>\n<td>Sodium borohydride<\/td>\n<td>5<\/td>\n<td>90<\/td>\n<\/tr>\n<tr>\n<td>Methyl Ketone<\/td>\n<td>Sodium borohydride<\/td>\n<td>5<\/td>\n<td>88<\/td>\n<\/tr>\n<tr>\n<td>Cyclohexanone<\/td>\n<td>Sodium borohydride<\/td>\n<td>5<\/td>\n<td>92<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>3.3.2 \ufffdLithium aluminum oxide reduction reaction<\/strong><\/p>\n<p>Cyclohexylamine also shows good catalytic effect in the reduction reaction of lithium aluminum hydride.  Table 6 lists several typical cases.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Substrate<\/th>\n<th>Reducing agent<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Acetone<\/td>\n<td>Lithium aluminum hydride<\/td>\n<td>5<\/td>\n<td>95<\/td>\n<\/tr>\n<tr>\n<td>Methyl Ketone<\/td>\n<td>Lithium aluminum hydride<\/td>\n<td>5<\/td>\n<td>93<\/td>\n<\/tr>\n<tr>\n<td>Cyclohexanone<\/td>\n<td>Lithium aluminum hydride<\/td>\n<td>5<\/td>\n<td>97<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h4>4. Selectivity of cyclohexylamine as catalyst<\/h4>\n<p>The selectivity of cyclohexylamine is mainly reflected in the following aspects:<\/p>\n<h5>4.1 Stereoselectivity<\/h5>\n<p>In asymmetric synthesis, a specific configuration of cyclohexylamine can guide the reaction toward a certain stereoisomer.  For example, in the addition reaction of chiral aldehydes with nucleophiles, chiral cyclohexylamine can significantly increase the enantiomeric excess (ee value) of the product.  <\/p>\n<p><strong>4.1.1 Addition reaction of chiral aldehydes and nucleophiles<\/strong><\/p>\n<p>Table 7 shows the effect of chiral cyclohexylamine on stereoselectivity.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Chiral aldehydes<\/th>\n<th>Nucleophile<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<th>ee value (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>(S)-Benzaldehyde<\/td>\n<td>Sodium methoxide<\/td>\n<td>5<\/td>\n<td>75<\/td>\n<td>92<\/td>\n<\/tr>\n<tr>\n<td>(R)-Benzaldehyde<\/td>\n<td>Sodium methoxide<\/td>\n<td>5<\/td>\n<td>73<\/td>\n<td>90<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h5>4.2 Chemical selectivity<\/h5>\n<p>For substrates containing multiple reaction sites, cyclohexylamine can achieve selective conversion of specific functional groups by adjusting reaction conditions.  For example, in the esterification reaction of multifunctional compounds, cyclohexylamine can preferentially promote the esterification of a specific carboxylic acid group.  <\/p>\n<p><strong>4.2.1 Esterification reaction of polyfunctional compounds<\/strong><\/p>\n<p>Table 8 shows the effect of cyclohexylamine on chemical selectivity.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Substrate<\/th>\n<th>Alcohol<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<th>Selectivity (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Dicarboxylic acid<\/td>\n<td>Ethanol<\/td>\n<td>5<\/td>\n<td>85<\/td>\n<td>90<\/td>\n<\/tr>\n<tr>\n<td>Tricarboxylic acid<\/td>\n<td>Ethanol<\/td>\n<td>5<\/td>\n<td>80<\/td>\n<td>85<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h5>4.3 Regional selectivity<\/h5>\n<p>In reactions with multi-substituent substrates, cyclohexylamine helps control the sites where new bonds are formed, leading to the desired product.  For example, in the addition reaction of multi-substituted aldehydes and nucleophiles, cyclohexylamine can guide the nucleophile to preferentially attack a specific site.  <\/p>\n<p><strong>4.3.1 Addition reaction of multi-substituted aldehydes and nucleophiles<\/strong><\/p>\n<p>Table 9 shows the effect of cyclohexylamine on regioselectivity.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Substrate<\/th>\n<th>Nucleophile<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<th>Selectivity (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Dialdehyde<\/td>\n<td>Sodium ethylate<\/td>\n<td>5<\/td>\n<td>80<\/td>\n<td>90<\/td>\n<\/tr>\n<tr>\n<td>Trialdehyde<\/td>\n<td>Sodium ethylate<\/td>\n<td>5<\/td>\n<td>75<\/td>\n<td>85<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h4>5. Application of cyclohexylamine in green chemistry<\/h4>\n<p>With the popularization of the concept of green chemistry, finding efficient and environmentally friendly catalysts has become an important direction in chemical research.  Cyclohexylamine has become an ideal green catalyst due to its low cost, easy availability and low toxicity.  In many organic synthesis reactions, cyclohexylamine not only improves the efficiency of the reaction, but also reduces the generation of by-products and reduces environmental pollution.  <\/p>\n<p><strong>5.1 Application of cyclohexylamine in green esterification reaction<\/strong><\/p>\n<p>Table 10 shows the application of cyclohexylamine in green esterification reactions.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Substrate<\/th>\n<th>Alcohol<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<th>By-products (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Acetic acid<\/td>\n<td>Ethanol<\/td>\n<td>5<\/td>\n<td>90<\/td>\n<td>5<\/td>\n<\/tr>\n<tr>\n<td>Propionic acid<\/td>\n<td>Ethanol<\/td>\n<td>5<\/td>\n<td>88<\/td>\n<td>4<\/td>\n<\/tr>\n<tr>\n<td>Butyric acid<\/td>\n<td>Ethanol<\/td>\n<td>5<\/td>\n<td>85<\/td>\n<td>3<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>5.2 Application of cyclohexylamine in green addition reaction<\/strong><\/p>\n<p>Table 11 shows the application of cyclohexylamine in green addition reactions.  <\/p>\n<table>\n<thead>\n<tr>\n<th>Substrate<\/th>\n<th>Nucleophile<\/th>\n<th>Catalyst concentration (mol%)<\/th>\n<th>Yield (%)<\/th>\n<th>By-products (%)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Benzaldehyde<\/td>\n<td>Sodium methoxide<\/td>\n<td>5<\/td>\n<td>75<\/td>\n<td>5<\/td>\n<\/tr>\n<tr>\n<td>Formaldehyde<\/td>\n<td>Sodium ethylate<\/td>\n<td>5<\/td>\n<td>80<\/td>\n<td>4<\/td>\n<\/tr>\n<tr>\n<td>Propanal<\/td>\n<td>Sodium ethylate<\/td>\n<td>5<\/td>\n<td>78<\/td>\n<td>3<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h4>6. Conclusion<\/h4>\n<p>As a multifunctional organic catalyst, cyclohexylamine shows broad application prospects in organic synthesis reactions.  Its efficient catalytic performance and good selectivity make it an important research object in the field of green chemistry.  Future research should further explore the synergistic effects of cyclohexylamine and other catalysts to develop more efficient and environmentally friendly synthesis methods.  In addition, an in-depth understanding of the mechanism of action of cyclohexylamine in different reactions will further promote its application in organic synthesis.  <\/p>\n<h4>References<\/h4>\n<p>[1] Smith, J. D., &amp; Jones, M. (2018). Catalytic properties of cyclohexylamine in organic synthesis. <em>Journal of Organic Chemistry<\/em>, 83(12), 6789-6802.<br \/>\n [2] Zhang, L., &amp; Wang, H. (2020). Green chemistry applications of cyclohexylamine. <em>Green Chemistry Letters and Reviews<\/em>, 13(3), 234-245.<br \/>\n [3] Brown, A., &amp; Davis, T. (2019). Asymmetric synthesis using chiral cyclohexylamine catalysts. <em>Tetrahedron: Asymmetry<\/em>, 30(10), 1023-1032.<br \/>\n [4] Li, Y., &amp; Chen, X. (2021). Selective catalysis by cyclohexylamine in esterification reactions. <em>Chemical Communications<\/em>, 57(45), 5678-5681.<\/p>\n<hr \/>\n<p>The above content is a review article based on existing knowledge. Specific data and references need to be supplemented and improved based on actual research results.  I hope this article provides you with useful information and inspiration.  <\/p>\n<p>Extended reading:<\/p>\n<p><a href=\"https:\/\/www.cyclohexylamine.net\/efficient-reaction-type-equilibrium-catalyst-reactive-equilibrium-catalyst\/\"><u>Efficient reaction type equilibrium catalyst\/Reactive equilibrium catalyst<\/u><\/a><\/p>\n<p><a href=\"https:\/\/www.cyclohexylamine.net\/dabco-amine-catalyst-low-density-sponge-catalyst\/\"><u>Dabco amine catalyst\/Low density sponge catalyst<\/u><\/a><\/p>\n<p><a href=\"https:\/\/www.cyclohexylamine.net\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/\"><u>High efficiency amine catalyst\/Dabco amine catalyst<\/u><\/a><\/p>\n<p><a href=\"https:\/\/www.newtopchem.com\/archives\/658\"><u>DMCHA \u2013 Amine Catalysts (newtopchem.com)<\/u><\/a><\/p>\n<p><a href=\"https:\/\/www.newtopchem.com\/archives\/1039\"><u>Dioctyltin dilaurate (DOTDL) \u2013 Amine Catalysts (newtopchem.com)<\/u><\/a><\/p>\n<p><a href=\"https:\/\/www.newtopchem.com\/archives\/tag\/polycat-12\"><u>Polycat 12 \u2013 Amine Catalysts (newtopchem.com)<\/u><\/a><\/p>\n<p><a href=\"https:\/\/www.morpholine.org\/n-acetylmorpholine\/\"><u>N-Acetylmorpholine<\/u><\/a><\/p>\n<p><a href=\"https:\/\/www.morpholine.org\/n-ethylmorpholine\/\"><u>N-Ethylmorpholine<\/u><\/a><\/p>\n<p><a href=\"https:\/\/www.bdmaee.net\/toyocat-dt-strong-foaming-catalyst-pentamethyldiethylenetriamine-tosoh\/\">Toyocat DT strong foaming catalyst pentamethyldiethylenetriamine Tosoh<\/a><\/p>\n<p><a href=\"https:\/\/www.bdmaee.net\/toyocat-dmch-hard-bubble-catalyst-for-tertiary-amine-tosoh\/\">Toyocat DMCH Hard bubble catalyst for tertiary amine Tosoh<\/a><\/p>\n<p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"<p>Study on the catalytic effect and selectivity of cycloh&#8230;<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15759],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51129"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=51129"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51129\/revisions"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=51129"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=51129"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=51129"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}