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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156218Generated: November 2, 2026

Sulfuryl chloride → 2-Chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoyl chloride

https://huagongshe.com/reaction/1156218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant2-Chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoic acidHCID 13013682—
Product2-Chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoyl chlorideHCID 1279963286%

Reaction Steps

In 100 ml sulfonylchloride was heated 20.0 g (0.057 mol) of 2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoic acid to reflux for 1 hour, and then thionylchloride was removed by distillation. By vacuum distillation of the residue, 18.2 g (0.049 mol) of 2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoyl chloride was obtained; yield 86.0%, b.p. 142°-155° C./0.35 mmHg, nD25 1.5652.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04334914
Source datasetuspto-grants-1982_06
ORD IDord-ca3e4616e49141b09e24d94846eca4ad
Source noteuspto-grants-1982_06