戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 569446作成日:2026年10月26日

Phosphorus oxychloride → HCID 131714060、化合物

https://huagongshe.com/reaction/569446

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxychlorideHCID 24813—
反応物Chloro-N,N-dimethylformiminium chlorideHCID 77311—
反応物Acetamide, 2-(trimethylsilyl)-HCID 357676—
反応物7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 12818006—
反応物4-Chloro-2-methoxycarbonylmethoxyimino-3-oxobutyric acidHCID 24820436—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 131714060HCID 13171406085%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04731443
出典データセットuspto-grants-1988_03
ORD IDord-4fddd52f64f94f689b9b6d6a9e648490
出典メモuspto-grants-1988_03