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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521183Generated: October 30, 2026

Sodium Thiosulfate → Benzo[b]thiophene, 5-bromo-, 1,1-dioxide

https://huagongshe.com/reaction/521183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-Bromo-1-benzothiopheneHCID 2776578—
SolventChloroformHCID 6212—
ProductBenzo[b]thiophene, 5-bromo-, 1,1-dioxideHCID 23261743—

Reaction Steps

5-Bromo-1-benzothiophene (1.50 g, 7.04 mmol) was dissolved in chloroform (47 mL) and allowed to stir vigorously at ambient temperature. m-CPBA (4.34 g, 17.6 mmol) was added in three portions and the resulting mixture was maintained at ambient temperature for 16 hours. The mixture was then diluted with 1M aqueous sodium thiosulfate and extracted with EtOAc. The organic layer was again washed with 1M aqueous sodium thiosulfate, saturated aqueous NaHCO3, brine, dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The residue was purified by MPLC on silica gel (using a gradient elution of 0-30% EtOAc/hexanes). Desired fractions were identified, combined, and concentrated in vacuo to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328099B2
Source datasetuspto-grants-2016_05
ORD IDord-bccfe4394601415e95306fa85873f336
Source noteuspto-grants-2016_05