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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1088084Erstellt: 26. Oktober 2026

Trifluoroacetic acid → 7-Amino-3vinyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1088084

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktSodium CarbonateHCID 10340—
EduktSodium BicarbonateHCID 516892—
EduktBenzhydryl 7-benzylideneamino-3-vinyl-3-cephem-4-carboxylateHCID 12818010—
LösungsmittelAnisoleHCID 7519—
LösungsmittelEthyl AcetateHCID 8857—
Produkt7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 1281800649,4%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04960889
Quelldatensatzuspto-grants-1990_10
ORD IDord-7856f0d74cfa4859a4be95e5e04cb44c
Quellennotizuspto-grants-1990_10