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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292342Generated: November 2, 2026

Trifluoroacetic acid → HCID 178460210, compound

https://huagongshe.com/reaction/2292342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHCID 178460209HCID 178460209—
SolventDichloromethaneHCID 6344—
ProductHCID 178460210HCID 178460210—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 10.83 g (13.6 mmol) of the crude [[[[[(S)-3-[[(Z)-(2-amino-4-thiazolyl)[(2-carboxy-2-methylethoxy)imino]acetyl]amino]-2-oxo-1-azetidinyl]carbonyl]amino]sulfonyl]amino]-3,4-dihydroxybenzeneacetic acid, diphenylmethyl ester in 45 ml of dry dichloromethane at -10° C., a cold solution of 11 ml of anisole in 110 ml of trifluoroacetic acid was added. After being stirred at 0° C. for 10 minutes, the clear solution was evaporated in vacuo at 0°-5° C. and the residue was treated with dry ether. The solid was collected by suction, washed with dry ether, dried in vacuo to give 7.28 g of impure [[[[[(S)-3-[[(Z)-(2-amino-4-thiazolyl)[(2-carboxy-2-methylethoxy)imino]acetyl]amino]-2-oxo-1-azetidinyl]carbonyl]amino]sulfonyl]amino]-3,4-dihydroxybenzeneacetic acid, trifluoroacetate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801705
Source datasetuspto-grants-1989_01
ORD IDord-bf767defe7964b1c8875609ddc0ee1c6
Source noteuspto-grants-1989_01