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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656198Generated: November 2, 2026

Trifluoroacetic acid → Unii-nyh6qmq9H0

https://huagongshe.com/reaction/1656198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantBenzhydryl 7-[2-(2-aminothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylateHCID 88469409—
SolventDichloromethaneHCID 6344—
ProductUnii-nyh6qmq9H0HCID 8846926040.2%

Reaction Steps

To a solution of benzhydryl 7-[2-(2-aminothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylate (6.79 g) in methylene chloride (68 ml) were added trifluoroacetic acid (29.1 g) and anisole (11.02 g) at 0° C., and the mixture was stirred at ambient temperature for 65 minutes. After the reaction mixture was evaporated, to the residue were added ethyl acetate and water, followed by adjusting to pH 7 with an aqueous solution of sodium bicarbonate. The separated aqueous solution was adjusted to pH 3.0 with 10% hydrochloric acid, and the precipitated substance was collected by filtration to give 7-[2-(2-aminothiazol-4yl)acetamido]-3-vinyl-3-cephem-4-carboxylic acid (1.88 g), mp 104°-116° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252731
Source datasetuspto-grants-1993_10
ORD IDord-4959c8f3417748a584c5e296526589c9
Source noteuspto-grants-1993_10