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HRID 1723540作成日:2026年10月27日

2,2-Dimethoxy-1-methylpyrrolidine → 1-(4-Methoxyphenyl)-3-(1-methyl-2-pyrrolidinylidene)-2(1H,3H)-indolone

https://huagongshe.com/reaction/1723540

反応式

関与物質

役割名称HCID仕込み量
反応物2,2-Dimethoxy-1-methylpyrrolidineHCID 11073552—
反応物1-(4-Methoxyphenyl)-1,3-dihydro-2H-indol-2-oneHCID 13339544—
溶媒ChloroformHCID 6212—
生成物1-(4-Methoxyphenyl)-3-(1-methyl-2-pyrrolidinylidene)-2(1H,3H)-indoloneHCID 54126479—

反応手順

1-(4-Methoxyphenyl)-2(1H,3H)-indolone (49 g, 0.205 mole), N-methyl-2-pyrrolidone dimethyl acetal (ca. 80%, 53 g, 0.245 mole, Ber, 97, pp. 3081-7, 1964) and 1000 ml chloroform were refluxed under nitrogen for 1.5 hours. The reaction mixture was cooled and evaporated in vacuo to solids. Two recrystallizations from ethyl acetate gave purified title product, 44.7 g, m.p. 90°-93° C. Thirty grams of this material were dried at 80° C./15 mm Hg for 20 hours to give 26.1 g of title product, m.p. 127°-9° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04861880
出典データセットuspto-grants-1989_08
ORD IDord-b84c88baecb24707a4e1d7024a20efe7
出典メモuspto-grants-1989_08