Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103138Generated: October 30, 2026

Boron tribromide → 4-Fluoro-5-(piperidine-1-sulfonyl)-benzene-1,2-diol

https://huagongshe.com/reaction/2103138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant1-(2-Fluoro-4,5-dimethoxy-benzenesulfonyl)-piperidineHCID 22475054—
SolventDichloromethaneHCID 6344—
Product4-Fluoro-5-(piperidine-1-sulfonyl)-benzene-1,2-diolHCID 2247507878%

Reaction Steps

A 1M solution of boron tribromide in dichloromethane (58 mL) was added dropwise to a cooled solution of 1-(2-fluoro-4,5-dimethoxy-benzenesulfonyl)-piperidine (5.89 g, 19.42 mmol) in dichloromethane (100 mL), maintaining the temperature between 10 and 20° C. The mixture was stirred overnight at room temperature and poured into 1M aqueous potassium dihydrogenphosphate and ice. After stirring 1 h, the phases were separated and the aqueous phase extracted with ethyl acetate. The combined organic phases were washed with brine, dried over magnesium sulfate and evaporated. The residue was purified by column chromatography on silica gel (10:1 dichloromethane/methanol eluant) to afford the title compound as a brown gum (4.17 g, 78%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576088B2
Source datasetuspto-grants-2009_08
ORD IDord-f8a7f59b0d4340668e15750a82b0532d
Source noteuspto-grants-2009_08