HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731692Generated: October 31, 2026
Trifluoroacetic acid → HCID 131714955, compound
https://huagongshe.com/reaction/1731692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131714956 | HCID 131714956 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 131714955 | HCID 131714955 | 43.3% |
Reaction Steps
To a suspension of benzhydryl 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-[(Z)-2-(3-pyridyl)vinylthiomethyl]-3-cephem-4-carboxylate (syn isomer) (1 g) in anisole (2.5 ml) was added trifluoroacetic acid (6 ml) under ice-cooling. The mixture was stirred for 40 minutes at ambient temperature, concentrated in vacuo to about a half volume and poured into diisopropyl ether (120 ml). The resulting precipitate was collected, dissolved in an aqueous solution (150 ml) of sodium bicarbonate (320 mg). The aqueous solution was washed with ethyl acetate and adjusted to pH 4-5 with 1N hydrochloric acid to give a precipitate. The precipitate was collected, washed with water and dried over phosphorus pentoxide to give 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-[(Z)-2-(3-pyridyl)vinylthiomethyl]-3-cephem-4-carboxylic acid (syn isomer) (330 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04622318 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-401ca6d772ed405ba382b23f9dcc9f9c |
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| Source note | uspto-grants-1986_11 |
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