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HRID 325420作成日:2026年10月26日

Diethyl acetonedicarboxylate → Ethyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetate

https://huagongshe.com/reaction/325420

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl acetonedicarboxylateHCID 66045—
反応物Sodium AcetateHCID 517045—
反応物HCID 178451312HCID 178451312—
触媒ZincHCID 23994—
溶媒Acetic AcidHCID 176—
生成物Ethyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetateHCID 5403425631%

反応手順

Crude t-butyl 5-(m-chlorophenyl)-2-hydroximino-3-oxopentanoate (43 g., 0.15 mol) and diethyl acetonedicarboxylate (28 ml, 30.3 g, 0.15 mol) are placed in a 1 liter round bottom flask and 250 ml of glacial acetic acid added. With stirring, 25 g (0.30 mol) anhydrous sodium acetate is added followed by 26 g Zn dust (94% fine, 0.364 mol) in a portionwise manner so that the exotherm does not bring the reaction to reflux. When addition is complete, the reaction is heated on a steam bath for one hour. The hot solution is then decanted from the residual zinc into 3 liters of ice water, and the resulting mixture is stirred vigorously until the oil solidifies. The mixture is then allowed to stand for 1.5 hours, and the solid is filtered. The solid is washed with water, dried in vacuo and recrystallized to give 21.5 g (31%) of ethyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetate, M.P. 131°- 132°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04440779
出典データセットuspto-grants-1984_04
ORD IDord-505488170c2b4d528249f20b4bfb6f2c
出典メモuspto-grants-1984_04