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HRID 280032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/280032

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 acidic 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US04587342
出典データセットuspto-grants-1986_05
ORD IDord-5465ba6dfefa4988b66fa1857a9e3d92
出典メモuspto-grants-1986_05