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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35247Generated: October 26, 2026

N-Methylcyclohexylamine → 4-Chloro-N-cyclohexyl-N-methylbutanamide

https://huagongshe.com/reaction/35247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-Chlorobutyryl chlorideHCID 78370—
SolventWaterHCID 962—
Product4-Chloro-N-cyclohexyl-N-methylbutanamideHCID 13208297—

Reaction Steps

To ethyl acetate (400 ml) is added N-methylcyclohexylamine (26 ml), and to the mixture are added dropwise with stirring 4-chlorobutyryl chloride (25 ml) and triethylamine (33.5 ml) over a period of 20 minutes with keeping the inner temperature at 10° to 20° C. by ice-cooling. The mixture is further stirred at room temperature for one hour. After the reaction, water is added to the reaction mixture. The organic layer is separated and washed with water an aqueious saturated potassium carbonate solution, 10% aqueous hydrochloric acid and water in order, and then dried over anhydrous sodium sulfate. After filtering off sodium sulfate, the mother liquor is concentrated and distilled under reduced pressure to give N-methyl-N-cyclohexyl-4-chlorobutyramide (41.5 g), b.p. 133°-136° C./2 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766120
Source datasetuspto-grants-1988_08
ORD IDord-d3926ad918984844bf5b7332cf93bba8
Source noteuspto-grants-1988_08