HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894850Generated: October 26, 2026
Water → N-[1-(Aminomethyl)cyclohexyl]aniline
https://huagongshe.com/reaction/1894850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Phenylamino-cyclohexanecarbonitrile | HCID 291030 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[1-(Aminomethyl)cyclohexyl]aniline | HCID 16227755 | 39.2% |
Reaction Steps
A solution of 5 g (25 mmol) of 1-phenylaminocyclohexanecarbonitrile in 70 ml of ethyl ether is added drop by drop to 1.13 g (29.8 mmol) of lithium aluminum hydride in 30 ml of ethyl ether at 0° C. The mixture is stirred for 2 hours at 0° C. The reaction is stopped by the addition of 1.1 ml of water, 1.1 ml of 15% sodium hydroxide and then 3.5 ml of water. The medium is then filtered on Celite and the filtrate is evaporated. The residue is purified on silica gel (dichloromethane then dichloromethane/methanol 80/20, v/v). 2 g of (1-aminomethylcyclohexyl)phenylamine are obtained in the form of a brown oil. Yield=39%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513307B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-0fe370108a194e3bac8bab05f99e79cd |
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| Source note | uspto-grants-2013_08 |
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