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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607943Generated: October 30, 2026

Trifluoroacetic acid → 7-Benzoylamino-3-chloromethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1607943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropyl EtherHCID 7914—
ReactantHexaneHCID 8058—
ReactantBenzhydryl 7-benzoylamino-3-chloromethyl-3-cephem-4-carboxylateHCID 67834587—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
Product7-Benzoylamino-3-chloromethyl-3-cephem-4-carboxylic acidHCID 67834677—

Reaction Steps

To a solution of benzhydryl 7-benzoylamino-3-chloromethyl-3-cephem-4-carboxylate (20 g) in a mixture of dichloromethane (40 ml) and anisole (10 ml) was added trifluoroacetic acid (20 ml) under cooling. After being stirred for two hours at -3°~0° C., the mixture was added dropwise to a mixture of diisopropyl ether (400 ml) and n-hexan (800 ml) at 5° C. The stirring was continued for 15 minutes at the same temperature. The resulting powder was collected by filtration, washed with n-hexan and dried over phosphorus pentoxide to give 7-benzoylamino-3-chloromethyl-3-cephem-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868174
Source datasetuspto-grants-1989_09
ORD IDord-0b2e1cfb68a548bfae26c0ea761ab83b
Source noteuspto-grants-1989_09