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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375729Generated: October 28, 2026

Thionyl Chloride → 3-(4-Trifluoromethylphenyl)-benzyl chloride

https://huagongshe.com/reaction/2375729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4'-(Trifluoromethyl)[1,1'-biphenyl]-3-methanolHCID 14468003—
SolventDichloromethaneHCID 6344—
Product3-(4-Trifluoromethylphenyl)-benzyl chlorideHCID 22280138—

Reaction Steps

The alcohol 2.2 (15 g, 59.5 mmol) was dissolved in anhydrous DCM (100 mL). Thionyl chloride (10 mL) was slowly added dropwise to the above solution. The resulting mixture was stirred at room temperature for 24 hours. The organic solvent was removed under vacuo. The residue was chromatographed (SiO2 gel 60, eluted with 20% DCM in hexanes). Fractions containing the desired product 2.3 were combined and concentrated to a white solid (14.0 g). 1H NMR (400 MHz) (CDCl3) δ 7.73 (4H, s); 7.65 (1H, s); 7.58 (1H, s); 7.52-7.28 (2H, m); 4.69 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465804B2
Source datasetuspto-grants-2008_12
ORD IDord-949ec55418034563ab0edd6d5205d4e8
Source noteuspto-grants-2008_12