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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292363Generated: October 31, 2026

Trifluoroacetic acid → HCID 131715844, compound

https://huagongshe.com/reaction/2292363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantThioanisoleHCID 7520—
ReactantHCID 131715845HCID 131715845—
SolventDiethyl EtherHCID 3283—
ProductHCID 131715844HCID 131715844—

Reaction Steps

At room temperature, 2.29 g (4 mmol) of (S)-[1-[[[[2-(2-bromo-4,5-dihydroxybenzoyl)hydrazino]sulfonyl]amino]carbonyl]-2-oxoazetidinyl]carbamic acid, phenylmethyl ester was added to a mixture of 4.5 ml of trifluoroacetic acid and 1.6 g of thioanisole. After stirring overnight, 50 ml of ether was added and the resulting crystals were filtered off by suction, dried and triturated with 40 ml of dichloromethane. The crystals were filtered off again and dried in vacuo; yield: 1.9 g, melting point 157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801705
Source datasetuspto-grants-1989_01
ORD IDord-0f30b5767587487bb0697118fdd3aee0
Source noteuspto-grants-1989_01