Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581805Generated: November 2, 2026

Boron tribromide → HCID 22723459, compound

https://huagongshe.com/reaction/1581805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 22723451HCID 22723451—
SolventDichloromethaneHCID 6344—
ProductHCID 22723459HCID 2272345976.2%

Reaction Conditions

Temperature-75 °C

Reaction Steps

A 70 ml CH2Cl2 suspension of 5-(2-methoxyphenyl)thiophene-2-sulfonamide (1.0 g, 3.7 mmol) is stirred under N2 at −75° C. as boron tribromide (1.1 ml, 12 mmol) is syringed into the reaction mixture. The amber solution is stirred for 30 minutes at −75° C., then at 0° C. for 2-3 hours. The reaction is quenched with ice, extracted with CH2Cl2. The extracts are washed with brine, dried (Na2SO4), filtered, and the filtrate is concentrated. The residue is purified by chromatography (SiO2, ethyl acetate/hexane gradient) to give 720 mg of 5-(2-hydroxyphenyl)thiophene-2-sulfonamide (76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730792B2
Source datasetuspto-grants-2004_05
ORD IDord-ac35cbc36348425693e01362cb3ec2f2
Source noteuspto-grants-2004_05