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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220282Generated: October 26, 2026

Chloroform → 3-Chloro-5-methyl-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophene

https://huagongshe.com/reaction/2220282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant5-Methyl-2-[2-(trifluoromethyl)[1,1'-biphenyl]-4-yl]-1-benzothiopheneHCID 68452800—
Product3-Chloro-5-methyl-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiopheneHCID 6845394356%

Reaction Steps

To a solution of 5-methyl-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophene (184 mg, 0.5 mmol) in CHCl3 (2.5 mL) is added SO2Cl2 (44 μL, 1.1 eq.). The mixture is heated to reflux overnight (about 14 hours). All the solvent is removed under reduced pressure. The residue is extracted with CH2Cl2 (50 mL), washed with saturated aqueous NaHCO3, brine, dried over MgSO4, filtered, and concentrated to give an oil. The mixture is purified by column chromatography (EtOAc/Hexane, gradient) to give 112 mg of 3-chloro-5-methyl-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophene in 56% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417065B2
Source datasetuspto-grants-2008_08
ORD IDord-979d7335e6914d85a7e9993265e5855e
Source noteuspto-grants-2008_08