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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13758Generated: October 29, 2026

Thionyl Chloride → 4-(1-Methylpiperidin-4-ylidenemethyl)-3-trifluoromethylbenzoyl chloride hydrochloride

https://huagongshe.com/reaction/13758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-(1-Methylpiperidin-4-ylidenemethyl)-3-trifluoromethylbenzoic acidHCID 23146000—
Product4-(1-Methylpiperidin-4-ylidenemethyl)-3-trifluoromethylbenzoyl chloride hydrochlorideHCID 23145987—

Reaction Steps

This compound was prepared in the same manner as in Reference Example 1 (step 7), except that 4-(1-methylpiperidin-4-ylidenemethyl)-3-trifluoromethylbenzoic acid obtained in the step 3 was used, and that treatment after the reaction was that thionyl chloride was distilled off under reduced pressure, and then the operation of adding of toluene to the residue, followed by azeotropic removal of thionyl chloride was repeated three times.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728131B2
Source datasetuspto-grants-2010_06
ORD IDord-2cdd0e5ba540401d9180b8b39a976552
Source noteuspto-grants-2010_06