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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654532Generated: October 31, 2026

Benzoyl chloride → HCID 178473102, compound

https://huagongshe.com/reaction/1654532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 178473103HCID 178473103—
SolventDichloromethaneHCID 6344—
ProductHCID 178473102HCID 178473102—

Reaction Steps

To an ice-cold mixture of 4.0 g. (10 mMol) ethyl trans-4-[2-(4-chlorobenzenesulphonylamino)-ethyl]-cyclohexyloxyacetate, 50 ml. methylene chloride and 1.5 g. (15 mMol) triethylamine is added dropwise a mixture of 1.4 g. (10 mMol) benzoyl chloride and 30 ml. methylene chloride. The reaction mixture is maintained for 4 hours at reflux temperature, cooled, filtered and the filtrate washed with dilute hydrochloric acid and water. It is then dried with anhydrous sodium sulphate and evaporated After purification over silica gel/ cyclohexane/diethyl ether (2:1 v/v), there is obtained a yield of 1.7 g (67% of theory); m.p. 81°-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407951
Source datasetuspto-grants-1995_04
ORD IDord-2b0432629a5f43768151d3ab04c20917
Source noteuspto-grants-1995_04