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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605584Generated: November 3, 2026

N-Methylcyclohexylamine → HCID 20318945, compound

https://huagongshe.com/reaction/1605584

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-chromatographically 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 numberUS03950393
Source datasetuspto-grants-1976_04
ORD IDord-17331bb8635b4278a4a1e4b46f3d925c
Source noteuspto-grants-1976_04