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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223248Generated: October 30, 2026

Benzoyl chloride → N-Cyclohexylbenzamide

https://huagongshe.com/reaction/223248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantCyclohexylamineHCID 7965—
SolventBenzeneHCID 241—
ProductN-CyclohexylbenzamideHCID 1565784%

Reaction Steps

18 g of cyclohexylamine was dissolved in 150 ml of benzene. To the resulting solution was very slowly added 20 g of benzoyl chloride with stirring at temperatures below 40° C. White crystals separated from the mixture, generating white smoke. The mixture was stirred for one hour and was then made alkaline by addition of pyridine thereto. The product was filtered with suction. Crude crystals melting at 142° C. to 144° C. were recrystallized from a mixture of methanol and ethanol (1:1 in volume), from which white needles melting at 144° C. to 145° C. separated. The yield was 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352860
Source datasetuspto-grants-1982_10
ORD IDord-0043fec0294648f3abdcc46f20d63d7f
Source noteuspto-grants-1982_10