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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834036Generated: October 30, 2026

Thionyl Chloride → HCID 21388394, compound

https://huagongshe.com/reaction/1834036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 21388393HCID 21388393—
SolventChloroformHCID 6212—
ProductHCID 21388394HCID 21388394—

Reaction Steps

11.45 g (0.096 mol) of freshly distilled thionyl chloride are added to a suspension of 28.65 g (0.077 mol) of 2-(4-chloro-phenyl)-2-(4-fluoro-3-trifluoromethylphenoxy)-acetic acid in 35 ml of dry chloroform. The mixture is stirred for 30 minutes at ambient temperature and is then heated at the reflux temperature until all the acid has dissolved (about 6 hours). The solution is evaporated to dryness under reduced pressure and 2-(4-chlorophenyl)-2-(4-fluoro-3-trifluoromethyl-phenoxy)-acetyl chloride is obtained in the form of an oil, which is used without further purification for the next stage of the synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067996
Source datasetuspto-grants-1978_01
ORD IDord-af4a0d2a9d6d4803a8bc98250bf22dea
Source noteuspto-grants-1978_01