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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295953Generated: October 31, 2026

Thionyl Chloride → 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chloride

https://huagongshe.com/reaction/2295953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantAcifluorfenHCID 44073—
SolventTolueneHCID 1140—
Product5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chlorideHCID 3017765—

Reaction Steps

2-Nitro-5-(2-chloro-4-trifluoromethylphenoxy)benzoic acid (80 grams) and toluene (80 ml) were charged into a reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. Thionyl chloride (80 ml) was slowly added at room temperature with stirring. After the addition was completed the mixture was heated at reflux with continued stirring for a period of one hour. Stirring was thereafter continued at room temperature overnight. Aftr this time the reaction mixture was stripped of toluene to yield the desired product 2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)benzoyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04427441
Source datasetuspto-grants-1984_01
ORD IDord-0c7550646ad841298e0a2f340e6b5ec4
Source noteuspto-grants-1984_01