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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494479Generated: October 30, 2026

Diketene → Benzhydryl 7-(4-bromoacetoacetamido)-3-methylthiomethyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1494479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiketeneHCID 12661—
ReactantBromineHCID 24408—
ReactantAcetamide, 2-(trimethylsilyl)-HCID 357676—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-3-oxobutanoyl bromideHCID 12831048—
ReactantBenzhydryl 7-amino-3-methylthiomethyl-3-cephem-4-carboxylateHCID 67712714—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzhydryl 7-(4-bromoacetoacetamido)-3-methylthiomethyl-3-cephem-4-carboxylateHCID 131713143—

Reaction Steps

To a solution of diketene (1.3 ml) in methylene chloride (10 ml) was added dropwise a solution of bromine (1.24 g) in methylene chloride (10 ml) at -30° C. with stirring, and the stirring was continued at -20° C. for half an hour to prepare a solution of 4-bromoacetoacetyl bromide. This solution was added dropwise to a solution of benzhydryl 7-amino-3-methylthiomethyl-3-cephem-4-carboxylate (4.44 g) and trimethylsilylacetamide (5.46 g) in methylene chloride (100 ml) at -30° to -20° C. over a period of 5 minutes with stirring, and the stirring was continued at -10° C. for half an hour. After addition of water, the resultant mixture was adjusted to pH 7.5 with an aqueous solution of sodium bicarbonate, followed by separating out the organic layer, which was washed with water and an aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and then evaporated to dryness to give benzhydryl 7-(4-bromoacetoacetamido)-3-methylthiomethyl-3-cephem-4-carboxylate (6.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026695
Source datasetuspto-grants-1991_06
ORD IDord-5766ffae32a14a78a869d8cbd595cb0b
Source noteuspto-grants-1991_06