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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978019Generated: October 27, 2026

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

https://huagongshe.com/reaction/978019

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 and aqueious saturated potassium carbonate solution, 10% 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 numberUS04663323
Source datasetuspto-grants-1987_05
ORD IDord-f2e6e344cebd4de4bcd21ac08395917a
Source noteuspto-grants-1987_05