戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 34470作成日:2026年10月26日

Acetic Acid → Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoate

https://huagongshe.com/reaction/34470

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Bromocresol GreenHCID 6451—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoateHCID 54507081—
溶媒EthanolHCID 702—
生成物Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoateHCID 20129780—

反応手順

A mixture of ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoate (19.8 g, 0.63 mole) in ethanol (500 mL) under nitrogen was treated with acetic acid (4 mL) and a trace of bromocresol green and heated to reflux. Heating was discontinued and sodium cyanoborohydride (4.4 g, 0.07 mole) in ethanol (100 mL) was co-added with additional acetic acid (11 mL). The mixture was stirred under nitrogen for 2 hr, acetic acid (10 mL) added and the ethanol removed under reduced pressure. The resultant yellow solid was taken up in ethyl acetate (250 mL) and successively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL), then dried over magnesium sulfate. The volatiles were removed under reduced pressure to leave an amber oil, 18.22 g (91.4%) which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04761475
出典データセットuspto-grants-1988_08
ORD IDord-62b182c93158406b8248468834a06f6a
出典メモuspto-grants-1988_08