Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925259Generated: October 29, 2026

Hydrochloric Acid → 2-[[3,3-Difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-benzoic acid

https://huagongshe.com/reaction/925259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Mercaptobenzoic AcidHCID 5443—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-Bromo-1,1-difluoropropyl)-4-fluorobenzeneHCID 67133822—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-[[3,3-Difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-benzoic acidHCID 8672016037%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2-mercapto-benzoic acid (0.10 g, 0.65 mmol) in acetone (30 ml) are added 1-(3-bromo-1,1-difluoro-propyl)-4-fluoro-benzene (0.16 g, 0.65 mmol) and potassium carbonate (0.27 g, 1.95 mmol) at RT. The reaction mixture is stirred at 70° C. for 2.5 h. The reaction mixture is diluted with water (20 ml), acidified with 2M hydrochloric acid and the aqueous layer is extracted with EtOAc (3×20 ml). The combined organic layers are washed with water (15 ml), brine (15 ml), dried over sodium sulfate and evaporated to dryness. The crude product is purified by column chromatography (silica gel, 80% EtOAc/hexane) to yield 2-[[3,3-difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-benzoic acid (0.08 g, 0.24 mmol, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284286B2
Source datasetuspto-grants-2016_03
ORD IDord-9a05a69ddfdc49daaf341e42d7076f62
Source noteuspto-grants-2016_03