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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716320Generated: October 31, 2026

Water → N-(4-Bromo-butyl)-2-(4-fluoro-benzenesulfonyl)-N-trityloxy-acetamide

https://huagongshe.com/reaction/1716320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-(4-Bromo-butyl)-2-(4-fluoro-phenylsulfanyl)-N-trityloxy-acetamideHCID 86619940—
SolventDichloromethaneHCID 6344—
ProductN-(4-Bromo-butyl)-2-(4-fluoro-benzenesulfonyl)-N-trityloxy-acetamideHCID 86619941—

Reaction Steps

N-(4-Bromo-butyl)-2-(4-fluoro-phenylsulfanyl)-N-trityloxy-acetamide from step D (105.2 mg, 0.182 mmol) and mCPBA (max. 77%, 0.21 g) in CH2Cl2 was stirred at room temperature for 30 min. The reaction was diluted with CH2Cl2 and water. The organic layer was sequentially washed with saturated Na2CO3 solution, 10% aqueous Na2SO3 and saturated Na2CO3 solution again. The organic phase was then dried and concentrated under the reduced pressure and purified by a column chromatography (0˜30% EtOAc in hexane). MS: 632.0, (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803793B2
Source datasetuspto-grants-2010_09
ORD IDord-b058ba553a584688b7471061afec3f45
Source noteuspto-grants-2010_09