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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647566Generated: October 30, 2026

Acetyl bromide → HCID 67712651, compound

https://huagongshe.com/reaction/647566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl bromideHCID 10482—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67712516HCID 67712516—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 67712651HCID 6771265192%

Reaction Steps

To a solution of benzhydryl 7-(2-phenylacetamido)-3-methylthiomethyl-3-cephem-4-carboxylate-1-oxide (15.1 g) in methylene chloride (150 ml) was added 2-methyl-2-butene (5.7 ml), followed by adding dropwise acetyl bromide (5.2 ml) under ice-cooling and stirring for half an hour. After addition of water, the mixture was adjusted to pH about 5 with an aqueous solution of sodium bicarbonate, washed three times with an aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and then evaporated under reduced pressure to give benzhydryl 7-[2-phenylacetamido]-3-methylthiomethyl-3-cephem-4-carboxylate (13.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04409215
Source datasetuspto-grants-1983_10
ORD IDord-4d406f1e1a484ea28ad111cc6ae7a1b0
Source noteuspto-grants-1983_10