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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435013Generated: October 29, 2026

Water → 4-Nitrobenzyl 7-[2-(2-bromoacetyl)acetamido]-3-cephem-4-carboxylate

https://huagongshe.com/reaction/435013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiketeneHCID 12661—
ReactantBromineHCID 24408—
Reactantp-Nitrobenzyl 7-amino-3-cephem-4-carboxylateHCID 12775080—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventAcetamide, 2-(trimethylsilyl)-HCID 357676—
SolventBistrimethylsilylacetamidHCID 11708267—
Product4-Nitrobenzyl 7-[2-(2-bromoacetyl)acetamido]-3-cephem-4-carboxylateHCID 8860774582.8%

Reaction Conditions

Temperature45 °C

Reaction Steps

4-Nitrobenzyl 7-amino-3-cephem-4-carboxylate (5 g.) was dissolved in a solution of trimethylsilylacetamide (13.8 g.) and bis(trimethylsilyl)acetamide (10 ml.) in dry ethyl acetate (50 ml.) and stirred at 45° C. for 1.5 hours. A solution of bromine (2.88 g.) in methylene chloride (7 ml.) was added dropwise to a solution of diketene (1.5 g.) in methylene chloride (7 ml.) at -40° C. over 20 minutes and stirred at -30° C. for 1 hour. The solution obtained thus was added to dropwise to the above solution of 4-nitrobenzyl 7-amino-3-cephem-4-carboxylate under cooling at -15° C. and then stirred at the same temperature for 30 minutes. Water (50 ml.) was added to the resultant solution and extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over magnesium sulfate and concentrated under reduced pressure to give oily 4-nitrobenzyl 7-[2-(2-bromoacetyl)acetamido]-3-cephem-4-carboxylate (6.15 g.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399133
Source datasetuspto-grants-1983_08
ORD IDord-ff09ed6f517547e8b5f9bd8150ad85d2
Source noteuspto-grants-1983_08