HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 647684Erstellt: 24. Oktober 2026
Trifluoroacetic acid → 7-Amino-3vinyl-3-cephem-4-carboxylic acid
https://huagongshe.com/de/reaction/647684
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | HCID 12818010 | HCID 12818010 | — |
| Lösungsmittel | Anisole | HCID 7519 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 7-Amino-3vinyl-3-cephem-4-carboxylic acid | HCID 12818006 | 49,4% |
Reaktionsschritte
To a suspension of benzhydryl 7-benzylideneamino-3-vinyl-3-cephem-4-carboxylate (8.6 g) in anisole (10 ml) was added dropwise trifluoroacetic acid (10 ml) at -20° C., and the reaction temperature was gradually raised to ambient temperature with stirring, followed by stirring at ambient temperature for half an hour. The reaction mixture was poured into a mixture of ethyl acetate (100 ml) and a saturated aqueous sodium bicarbonate (100 ml), and then the mixture was adjusted to pH 7.5 with 20% aqueous sodium carbonate. The separated aqueous solution was washed with ethyl acetate (100 ml) and adjusted to pH 7.2 with conc. hydrochloric acid, followed by subjecting to column chromatography on alumina (10 ml). Elution was carried out with 15% aqueous sodium chloride, and fractions containing a desired compound were collected and then adjusted to pH 3.3 with conc. hydrochloric acid. The precipitated crystals were collected by filtration, washed with acetone and dried to obtain 7-amino-3-vinyl-3-cephem-4-carboxylic acid (2.0 g), mp 200°-230° C. (dec.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04409214 |
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| Quelldatensatz | uspto-grants-1983_10 |
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| ORD ID | ord-06c9b378f5a24f0d8d2c66c4312a8f9f |
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| Quellennotiz | uspto-grants-1983_10 |
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