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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391247Generated: October 31, 2026

Thionyl Chloride → 5-(3-Chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoyl chloride

https://huagongshe.com/reaction/391247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-(3-Chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoic acidHCID 57572841—
SolventTolueneHCID 1140—
Product5-(3-Chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoyl chlorideHCID 57572840—

Reaction Steps

5-(3-Chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoic acid (10 g) was suspended in toluene (50 ml) with stirring at room temperature, thionyl chloride (4.57 g) was added dropwise at 65-75° C., and the mixture was stirred for 1.5 hr. After cooling, the solvent was concentrated under reduced pressure, toluene (50 ml) was added to the residue, and the mixture was concentrated again under reduced pressure. The residue was dissolved in toluene (20 ml) to give a solution of 5-(3-chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoyl chloride in toluene. This was identified as the title compound by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383819B2
Source datasetuspto-grants-2013_02
ORD IDord-3e78f13e69d34d57ad6ca2a1f6b19f81
Source noteuspto-grants-2013_02