Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866952Generated: October 30, 2026

N-Methylcyclohexylamine → HCID 20318945, compound

https://huagongshe.com/reaction/866952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantHCID 18629983HCID 18629983—
SolventChloroformHCID 6212—
ProductHCID 20318945HCID 20318945—

Reaction Steps

48 gm of N-methyl-cyclohexylamine were added to 56 gm of 4-acetylamino-3-tert.butyl-benzyl bromide in 500 ml of chloroform, and the mixture was refluxed for 1.5 hours. Subsequently, the reaction mixture was extracted three times with water, and the organic phase was evaporated. The residue was purified column-chromatography on silicagel with chloroform/methanol (5:1), and 4-acetylamino-3-tert.butyl-N-cyclohexyl-N-methyl-benzylamine hydrochloride, m.p. 240°-243° C (decomp.), was crystallized from a solution of the purified base in absolute ethanol/ether by addition of absolute ethanolic hydrochloric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101671
Source datasetuspto-grants-1978_07
ORD IDord-5eb86be7e49a4f0aa175410267a393d8
Source noteuspto-grants-1978_07