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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249619Generated: October 31, 2026

Trifluoroacetic acid → HCID 178511446, compound

https://huagongshe.com/reaction/249619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178453837HCID 178453837—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
ProductHCID 178511446HCID 17851144667.4%

Reaction Steps

To a solution of 7β-(N-t-butoxycarbonyl-2-phenylglycylamino) -3- (trityl-1,2,3-triazol-4-ylthiomethylthio) -3-cephem-4-carboxylic acid diphenylmethyl ester (480 mg : 0.487 mMol.) in a mixture of anisole (1.2 ml) and dichloromethane (3 ml) under ice cooling is added trifluoro- acetic acid (3 ml), and the mixture is stirred under ice cooling for 30 minutes and at room temperature for 50 minutes. The reaction mixture is shaken with ice water and ethyl acetate under ice cooling. The aqueous layer is taken, concentrated to remove the remaining organic solvents under reduced pressure, and subjected to column chromatography over styrene-divinylbenzene copolymer resin (methanol : water=4:1). The residue is pulverized from ethyl acetate to give 7β-(2-phenylglycylamino)-3-(1,2,3-triazol -4-ylthiomethylthio)-3-cephem-4-carboxylic acid (157 mg) as white powder. Yield: 67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214037
Source datasetuspto-grants-1993_05
ORD IDord-3b2470d23ee9439a9982dc3a201ebf5c
Source noteuspto-grants-1993_05