Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34071Generated: October 29, 2026

Sodium Thiosulfate → (5-Bromo-2-chlorothiophen-3-yl)methanol

https://huagongshe.com/reaction/34071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
Reactant(2-Chlorothiophen-3-yl)methanolHCID 18938072—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(5-Bromo-2-chlorothiophen-3-yl)methanolHCID 2307016080.6%

Reaction Steps

To a solution of 3.0 g of (2-chlorothiophen-3-yl)methanol in 60 mL of dimethylformamide was added 3.59 g of N-bromosuccinimide at room temperature, and stirred at this temperature for 2 hours. Adding 10 mL of 10% sodium thiosulfate, and the resultant solution was diluted with ethyl acetate. The organic layer was washed successively with saturated aqueous ammonium chloride and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated, to afford 3.7 g of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429609B2
Source datasetuspto-grants-2008_09
ORD IDord-f574309933cb4930a12807a587ce64b2
Source noteuspto-grants-2008_09