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HRID 1638452作成日:2026年10月25日

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

https://huagongshe.com/reaction/1638452

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US04879391
出典データセットuspto-grants-1989_11
ORD IDord-8d039b96c52c4204babea6ff1ea17f6c
出典メモuspto-grants-1989_11