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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288294Generated: October 31, 2026

Cyclohexanone → 1-Aminocyclohexanecarbonitrile

https://huagongshe.com/reaction/2288294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantSodium CyanideHCID 8929—
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium ChlorideHCID 25517—
SolventWaterHCID 962—
Product1-AminocyclohexanecarbonitrileHCID 7963589.6%

Reaction Steps

1.23 g of sodium cyanide, 1.58 g of ammonium chloride and 8 ml of ammonium hydroxide are introduced, the whole is taken to 0° C. and 2.1 g of cyclohexanone is added. The reaction medium is left to return to ambient temperature under agitation for 18 hours, diluted in a small amount of water and decanted. The aqueous phase is extracted with methylene chloride, the organic phases are combined, washed with salt water, dried, filtered and concentrated. In this way 2.38 g of expected product (colourless oil) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087509
Source datasetuspto-grants-2000_07
ORD IDord-760aa3e0bcd842e5aa262a391e842d4b
Source noteuspto-grants-2000_07