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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325420생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/325420

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl acetonedicarboxylateHCID 66045—
반응물Sodium AcetateHCID 517045—
반응물HCID 178451312HCID 178451312—
촉매ZincHCID 23994—
용매Acetic AcidHCID 176—
생성물Ethyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetateHCID 5403425631%

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04440779
출처 데이터셋uspto-grants-1984_04
ORD IDord-505488170c2b4d528249f20b4bfb6f2c
출처 메모uspto-grants-1984_04