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HRID 647684作成日:2026年10月26日

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

https://huagongshe.com/reaction/647684

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Sodium CarbonateHCID 10340—
反応物Sodium BicarbonateHCID 516892—
反応物Benzhydryl 7-benzylideneamino-3-vinyl-3-cephem-4-carboxylateHCID 12818010—
溶媒AnisoleHCID 7519—
溶媒Ethyl AcetateHCID 8857—
生成物7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 1281800649.4%

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04409214
出典データセットuspto-grants-1983_10
ORD IDord-06c9b378f5a24f0d8d2c66c4312a8f9f
出典メモuspto-grants-1983_10