戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 569350作成日:2026年10月27日

p-Toluenesulfonic acid → 7-Amino-3vinyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/569350

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Ethyl AcetateHCID 8857—
反応物Sodium CarbonateHCID 10340—
反応物Benzhydryl 7-amino-3vinyl-3cephem-4-carboxylate hydrochlorideHCID 12818005—
溶媒MethanolHCID 887—
溶媒AnisoleHCID 7519—
生成物7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 1281800660.8%

反応条件

温度50 °C

反応手順

To a suspension of benzhydryl 7-amino-3-vinyl-3-cephem-4-carboxylate hydrochloride (48 g) in methanol (250 ml) and anisole (70 ml) was added p-toluenesulfonic acid (85 g), and the mixture was stirred at 50° C. for 2 hours. The reaction mixture was poured into 10% aqueous sodium carbonate (600 ml) and ethyl acetate (700 ml), followed by adjusting to pH 7.5 with 20% aqueous sodium carbonate. The separated aqueous solution was washed with ethyl acetate (500 ml) and then adjusted to pH 2.5 with conc. hydrochloric acid, followed by stirring under ice-cooling for an hour. The precipitated crystals were collected by filtration and washed with acetone to obtain 7-amino-3-vinyl-3-cephem-4-carboxylic acid (15.4 g), mp 200° to 230° C. (dec.).

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-e9b803ed96ae48b691fc861dea4e89f6
出典メモuspto-grants-1988_03