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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905403생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/905403

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Sodium CarbonateHCID 10340—
반응물Sodium BicarbonateHCID 516892—
반응물Benzhydryl 7-benzylideneamino-3-vinyl-3-cephem-4-carboxylateHCID 12818010—
용매AnisoleHCID 7519—
용매Ethyl AcetateHCID 8857—
생성물7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 1281800649.4%

반응 단계

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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04423213
출처 데이터셋uspto-grants-1983_12
ORD IDord-6fe1a1be03274d3b88d517b5052eafd4
출처 메모uspto-grants-1983_12