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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290683Generated: October 31, 2026

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

https://huagongshe.com/reaction/2290683

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. After this time the reaction mixture was stripped of toluene to yield the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04618359
Source datasetuspto-grants-1986_10
ORD IDord-a4c4c3342db04ceb84c38365d763ccc8
Source noteuspto-grants-1986_10