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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371860Generated: October 31, 2026

N-Methylcyclohexylamine → HCID 20318945, compound

https://huagongshe.com/reaction/371860

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-chromatograhically 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 numberUSRE029628
Source datasetuspto-grants-1978_05
ORD IDord-aadb56c5e4c24642b713e05e462191a6
Source noteuspto-grants-1978_05