Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381387Generated: November 1, 2026

Trifluoroacetic acid → 7-(4-Bromo-2-methoxyiminoacetoacetamido)-3-vinyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1381387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantBenzhydryl 7-(4-bromo-3,3-diethoxy-2-methoxyiminobutyramido)-3-vinyl-3-cephem-4-carboxylateHCID 131713161—
SolventDichloromethaneHCID 6344—
Product7-(4-Bromo-2-methoxyiminoacetoacetamido)-3-vinyl-3-cephem-4-carboxylic acidHCID 13171316274.1%

Reaction Steps

To a solution of benzhydryl 7-(4-bromo-3,3-diethoxy-2-methoxyiminobutyramido)-3-vinyl-3-cephem-4-carboxylate (syn isomer) (3.36 g) and anisole (2.1 g) in methylene chloride (20 ml) was added trifluoroacetic acid (8.0 g) under ice-cooling with stirring, and the stirring was continued at ambient temperature for an hour. After removal of the solvent, the residue was dissolved in a mixture of ethyl acetate and water. To the separated ethyl acetate solution was added water, followed by adjusting to pH 7 with a saturated aqueous sodium bicarbonate. To the separated aqueous solution was added ethyl acetate, followed by adjusting to pH 2 with 10% hydrochloric acid. The ethyl acetate layer was separated out, washed with an aqueous sodium chloride and then dried over anhydrous magnesium sulfate. Removal of the solvent gave 7-(4-bromo-2-methoxyiminoacetoacetamido)-3-vinyl-3-cephem-4-carboxylic acid (syn isomer) (1.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585860
Source datasetuspto-grants-1986_04
ORD IDord-698ae8334e86485b98cd589a95a77261
Source noteuspto-grants-1986_04