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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863355Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 57294913, compound

https://huagongshe.com/reaction/863355

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant4-nitrobenzyl (1R,5S,6S)-2-(2-diethylcarbamoylphenylthio)-1-methyl-6-[1(R)-trimethylsilyloxyethyl]-1-carbapen-2-em-3-carboxylateHCID 9960788—
SolventDichloromethaneHCID 6344—
ProductHCID 57294913HCID 5729491383.4%

Reaction Steps

122 mg (1.45 mmol) of sodium hydrogencarbonate were added to 6 ml of a methylene chloride solution containing 304 mg (0.486 mmol) of 4-nitrobenzyl (1R,5S,6S)-2-(2-diethylcarbamoylphenylthio)-1-methyl-6-[1(R)-trimethylsilyloxyethyl]-1-carbapen-2-em-3-carboxylate (prepared as described in Example 34). The mixture was then placed in an ice bath while 105 mg (0.487 mmol) of m-chloroperbenzoic acid (80% purity) were added, with stirring. The reaction mixture was stirred for 1 hour at the same temperature, after which it was diluted with methylene chloride and washed with an ice-cooled dilute aqueous solution of sodium hydrogencarbonate. The solvent was then removed by distillation under reduced pressure. The resulting residue was purified by column chromatography through 25 g of silica gel. Elution with a 2:1 by volume mixture of ethyl acetate and hexane afforded 260 mg (yield 83%) of the title compound as a foam-like solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719275
Source datasetuspto-grants-1998_02
ORD IDord-4514992643a34392926abb7caf05fe7a
Source noteuspto-grants-1998_02