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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202605Generated: November 2, 2026

Thionyl Chloride → 1-(Chlorophenylmethyl)-4-fluorobenzene

https://huagongshe.com/reaction/2202605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-FluorobenzhydrolHCID 570753—
SolventDichloromethaneHCID 6344—
Product1-(Chlorophenylmethyl)-4-fluorobenzeneHCID 21625695.2%

Reaction Steps

In dichloromethane (30 mL), (±)-(4-fluorophenyl)phenylmethanol (2.1 g, 10 mmol) synthesized in Production Example 195 was dissolved, and thionyl chloride (5.1 g, 42 mmol) was added dropwise thereto at a room temperature. After the completion of the dropping, the mixture was heated under reflux, and the completion of the reaction was confirmed by TLC. After the completion of the reaction, the reaction mixture was concentrated, diluted with ethyl acetate, and washed with water. The organic layer was dried over magnesium sulfate, and the solvent was distilled off. Thus the title compound (2.1 g, 94%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365553B2
Source datasetuspto-grants-2016_06
ORD IDord-5873cc4dd1494309bcc9ab90319b79c8
Source noteuspto-grants-2016_06