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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719575Generated: November 4, 2026

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

https://huagongshe.com/reaction/1719575

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 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04540703
Source datasetuspto-grants-1985_09
ORD IDord-e7252266dd6c4cc4b55b7603db78d91b
Source noteuspto-grants-1985_09