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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560082Generated: October 30, 2026

Iodine → 1-Benzenesulfonyl-2-(4-bromo-phenyl)-aziridine

https://huagongshe.com/reaction/560082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDichloromethaneHCID 6344—
Reactant4-BromostyreneHCID 16263—
ReactantChloramine BHCID 4347343—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-Benzenesulfonyl-2-(4-bromo-phenyl)-aziridineHCID 4684566948.7%

Reaction Steps

To a stirred suspension of chloramine B (CAS [127-52-6], 1.35 g) in acetonitrile (18 mL) under argon was added iodine (0.16 g). 4-Bromostyrene (2.41 g) was added and the mixture was stirred for 19 h at room temperature. Dichloromethane (240 mL) and water (120 mL) were added and the mixture was extracted with dichloromethane. The org. phase was washed with water and brine, dried over MgSO4 and K2CO3 and filtered. The filtrate was concentrated and the product was purified using column chromatography (SiO2, cyclohexane/ethyl acetate 95:5=>ethyl acetate) to give 1-benzenesulfonyl-2-(4-bromo-phenyl)-aziridine (1.04 g) as a colorless oil. MS: 340.0 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063088B2
Source datasetuspto-grants-2011_11
ORD IDord-544429e502314da8a3d57eaade455ae0
Source noteuspto-grants-2011_11