HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249619Generated: November 1, 2026
Trifluoroacetic acid → HCID 178511446, compound
https://huagongshe.com/reaction/249619
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 178453837 | HCID 178453837 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 178511446 | HCID 178511446 | 67.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214037 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-3b2470d23ee9439a9982dc3a201ebf5c |
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| Source note | uspto-grants-1993_05 |
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