HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081563Generated: November 1, 2026
Trifluoroacetic acid → HCID 178496724, compound
https://huagongshe.com/reaction/1081563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 23362766 | HCID 23362766 | — |
| Reactant | HCID 70062891 | HCID 70062891 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178496724 | HCID 178496724 | — |
Reaction Steps
A solution of 2-bromo-4-tert-butylcarbonyl-7α-methoxy-3-methyl-3-cephem 1,1-dioxide (110 mg) in acetonitrile (100 ml) was treated with 4-[(6-benzhydryloxy-2,5-dihydro-2-methyl-5-oxo-1,2,4- triazin-3-yl)thiomethyl]benzoic acid siver salt (230 mg). The reaction mixture was stirred at room temperature for 30 minutes, then diluted with EtOAC, filtered and rotoevaporated. Upon purification of the residue by flash chromatography 4-tert-butylcarbonyl-2-{4-[(6-benzhydryloxy-2,5-dihydro-2-methyl-5-oxo-1,2,4-triazin-3-yl)thiomethyl]benzoyloxy}-7α-methoxy-3-methyl-3-cephem 1,1-dioxide was obtained as a white solid (mg 75). This product was dissolved in methylene chloride (0.5 ml) and sequentially treated with anisole (0.03 ml) and trifluoroacetic acid (0.5 ml).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05587373 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-db6f8104abbc4e7697703b4551aae18f |
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| Source note | uspto-grants-1996_12 |
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