Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647568Generated: October 26, 2026

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

https://huagongshe.com/reaction/647568

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 numberUS04409215
Source datasetuspto-grants-1983_10
ORD IDord-1716a558afb9403fab10b138d3b4a5ec
Source noteuspto-grants-1983_10