Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900086Generated: November 1, 2026

Water → 4-(4-Cyano-cyclohexyl)-aniline

https://huagongshe.com/reaction/1900086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ChlorideHCID 5234—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant4-(4-Aminophenyl)cyclohexan-1-oneHCID 23371894—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(4-Cyano-cyclohexyl)-anilineHCID 2337186956%

Reaction Steps

392 mg (3.5 mmol) of potassium t-butylate were added portionwise at -10° to a suspension of 278 mg (1.5 mmol) of 4-(4-oxo-cyclohexyl)-aniline and 370 mg (1.9 mmol) of toluene-4-sulfonylmethylisocyanide in 5 ml of 1,2-dimethoxyethane and 0.15 ml of ethanol. After stirring at -5° for 1 hour and at room temperature for a further 70 hours 25 ml of water and 10 ml of saturated sodium chloride solution were added and the mixture was extracted three times with 40 ml of dichloromethane each time. The organic phase was dried with sodium sulfate and concentrated. Chormatography over silica gel with ethyl acetate/hexane 1:2 gave 165 mg (56%) of 4-(4-cyano-cyclohexyl)-aniline with m.p. 132°-140°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574055
Source datasetuspto-grants-1996_11
ORD IDord-eac76925a80c4474b63b144e45559c3a
Source noteuspto-grants-1996_11