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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397457Generated: October 31, 2026

Trifluoroacetic acid → HCID 21438364, compound

https://huagongshe.com/reaction/2397457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 21438369HCID 21438369—
ProductHCID 21438364HCID 21438364—

Reaction Steps

A solution of 3.29 g. of 1-methyl-4-(2-trifluoromethylthio-9-hydroxythioxanthen-9yl)piperidine in 15 ml. of trifluoroacetic anhydride and 30 ml. of trifluoroacetic acid is stirred and refluxed for 2.5 hours. The solution is evaporated to dryness. The residue is dissolved in benzene and is washed with 10% sodium hydroxide to make the free base form. The benzene is washed with water, dried over magnesium sulfate, filtered, and the benzene is removed on a rotary evaporator. The residue is recrystallized from acetonitrile to give 1-methyl-4-[2-(trifluoromethylthio)thioxanthen-9-ylidene]piperidine, m.p. 104°-106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04021561
Source datasetuspto-grants-1977_05
ORD IDord-460e70d81d9d44cf9d426c770b3a8d2d
Source noteuspto-grants-1977_05