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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902918Generated: October 25, 2026

N-bromobutanimide → HCID 70463851, compound

https://huagongshe.com/reaction/1902918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantTrimethylsilyl (trimethylsilyl)sulphamateHCID 87497—
Reactant7-Benzamido-3-methyl-3-cephem-4-carboxylic acid-1-oxideHCID 70464702—
SolventDichloromethaneHCID 6344—
ProductHCID 70463851HCID 7046385149%

Reaction Conditions

Temperature40 °C

Reaction Steps

207 mg (0.86 mmoles) of trimethylsilyl trimethylsilylamidosulfonate were added to a suspension of 353 mg (1.06 mmoles) of 7-benzamido-3-methyl-3-cephem-4-carboxylic acid-1-oxide in 25 ml of dichloromethane and the mixture was stirred at 40° C. for 3 hours. The colorless translucent suspension was cooled in an ice-bath and bromination was carried out in half an hour using 277 mg of N-bromosuccinimide (1.56 mmoles) as the brominating agent to obtain a 49% yield of trimethylsilyl 7-benzamido-3-bromomethyl-3-cephem-4-carboxylate-1-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04366315
Source datasetuspto-grants-1982_12
ORD IDord-c732612f6c1e4a09bb0b29815df1ca69
Source noteuspto-grants-1982_12