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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284007Generated: October 31, 2026

Trifluoroacetic acid → HCID 21515344, compound

https://huagongshe.com/reaction/1284007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86733870HCID 86733870—
CatalystAnisoleHCID 7519—
ProductHCID 21515344HCID 21515344—

Reaction Steps

3.92 g. (10 mM) of the benzhydryl ester from Example 2 are stirred together with 30 ml. of trifluoroacetic acid and a few drops of anisole at 0° for 10 minutes. After distilling the solvent off in vacuum, the residue is treated with petroleum ether until it becomes solid. The solid is then stirred for five minutes in 50 ml. of sodium bicarbonate and filtered. After acidification with 2 N hydrochloric acid and extraction twice, each time with 20 ml. of ether and then drying from the organic phase, 1.2 g. of α-[(methoxycarbonothioyl)oxy]benzeneacetic acid are obtained from the filtrate in the form of white crystals after crystallization from cyclohexane/benzol, m.p. 86°-87°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978050
Source datasetuspto-grants-1976_08
ORD IDord-25f2753acb7a465e83c2672fb985721d
Source noteuspto-grants-1976_08