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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605583Generated: October 31, 2026

N-Methylcyclohexylamine → HCID 20319113, compound

https://huagongshe.com/reaction/1605583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantHCID 20318965HCID 20318965—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 20319113HCID 20319113—

Reaction Steps

24 gm of N-methyl-cyclohexylamine were added to 23 gm of 2-acetylamino-5-tert.butyl-benzylbromide in 1.6 liters of carbon tetrachloride, and the mixture was refluxed for 1 hour. After cooling, the precipitated N-methyl-cyclohexylamine hydrobromide was filtered off, the filtrate was evaporated, and the crude product was purified chromatographically on silicagel with ethyl acetate. The corresponding fractions were combined and evaporated, and the 2-acetylamino-5-tert.butyl-N-cyclohexyl-N-methyl-benzylamine thus obtained was recrystallized from petroleum ether, whereupon it had a melting point of 111°-112.5°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950393
Source datasetuspto-grants-1976_04
ORD IDord-bd8863a1fbfd4588a5c7abcb4a87b911
Source noteuspto-grants-1976_04