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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292371Generated: October 30, 2026

Trifluoroacetic acid → HCID 131715847, compound

https://huagongshe.com/reaction/2292371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodiumHCID 5360545—
ReactantHCID 131715848HCID 131715848—
SolventThioanisoleHCID 7520—
ProductHCID 131715847HCID 131715847—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 20 ml of thioanisole and 75 ml of trifluoroacetic acid was cooled to 0° C. and 15.25 g of (S)-[1-[[[[[[3-(3,4-dihydroxyphenyl)-2-oxo-1-imidazolidinyl]carbonyl]amino]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, phenylmethyl ester, monosodium salt was added. After stirring overnight at room temperature, the excess trifluoroacetic acid was evaporated in vacuo and the residue triturated with ether. The precipitate was filtered off by suction, washed with ether, and dried in vacuo; yield: 15.69 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801705
Source datasetuspto-grants-1989_01
ORD IDord-16b0e41fedb040bbb386b4024e60d2c4
Source noteuspto-grants-1989_01