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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292338Generated: November 1, 2026

Trifluoroacetic acid → HCID 131715834, compound

https://huagongshe.com/reaction/2292338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantThioanisoleHCID 7520—
ReactantHCID 131715835HCID 131715835—
SolventDiethyl EtherHCID 3283—
ProductHCID 131715834HCID 131715834—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a mixture of 12 ml of trifluoroacetic acid and 3 ml of thioanisole was added 2.92 g (4.94 mmol) of (S)-[1-[[[[4-[(3,4-dihydroxybenzoyl)amino]-2,3-dioxo-1-piperazinyl]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, phenylmethyl ester at 0° C. After stirring overnight at 10° C., 150 ml of ether was added and the resulting precipitate was filtered off, washed with ether and dried in vacuo. For further purification, the salt was triturated two times with dichloromethane; yield: 2.56 g; melting point 206°-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801705
Source datasetuspto-grants-1989_01
ORD IDord-c81fbce4c1ad4fb0a01665a9d81f956e
Source noteuspto-grants-1989_01