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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569446생성일: 2026년 10월 25일

Phosphorus oxychloride → HCID 131714060, 화합물

https://huagongshe.com/reaction/569446

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물Chloro-N,N-dimethylformiminium chlorideHCID 77311—
반응물Acetamide, 2-(trimethylsilyl)-HCID 357676—
반응물7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 12818006—
반응물4-Chloro-2-[(2-methoxy-2-oxoethoxy)imino]-3-oxobutanoic acidHCID 24820436—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물HCID 131714060HCID 13171406085%

반응 단계

Vilsmeier reagent prepared from N,N-dimethylformamide (3.76 ml) and phosphorus oxychloride (4.46 ml) was suspended in dry tetrahydrofuran (50 ml). To the suspension was added 4-chloro-2-methoxycarbonylmethoxyimino-3-oxobutyric acid (syn isomer) (10.5 g), and the mixture was stirred under ice-cooling to prepare the activated acid solution. This solution was added at a time to a solution of 7-amino-3-vinyl-3-cephem-4-carboxylic acid (10 g) and trimethylsilylacetamide (35 g) in ethyl acetate (110 ml) at -30° C. After the reaction mixture was stirred at -15° C. for an hour, the resultant solution was poured into water (100 ml) and then extracted with ethyl acetate (200 ml). The extract was washed with a saturated aqueous sodium chloride and dried over magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was triturated with diisopropyl ether to give 7-(4-chloro-2-methoxycarbonylmethoxyimino-3-oxobutyramido)-3-vinyl-3-cephem-4-carboxylic acid (syn isomer) (16.75 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04731443
출처 데이터셋uspto-grants-1988_03
ORD IDord-4fddd52f64f94f689b9b6d6a9e648490
출처 메모uspto-grants-1988_03