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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 342963생성일: 2026년 10월 25일

Diisopropylamine → Ethyl 1-(3-(tert-butoxy)-3-oxopropanoyl)cyclopropane-1-carboxylate

https://huagongshe.com/reaction/342963

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물tert-Butyl acetateHCID 10908—
반응물Ammonium ChlorideHCID 25517—
반응물Diethyl cyclopropane-1,1-dicarboxylateHCID 73790—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물Ethyl 1-(3-(tert-butoxy)-3-oxopropanoyl)cyclopropane-1-carboxylateHCID 5407134845.6%

반응 조건

온도-78 °C

반응 단계

A solution of n-butyllithium (2.5M in hexane, 40 ml) was added dropwise with stirring to a cooled solution of diisopropylamine (10.1 g) in anhydrous ether (100 ml) in an atmosphere of nitrogen, whilst maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 5 hour and a solution of t-butyl acetate (11.6 g) in anhydrous ether (20 ml) was added dropwise, whilst maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 1 hour and a solution of diethyl cyclopropane-1,1-dicarboxylate (18.6 g) in anhydrous ether (20 ml) was added dropwise whilst maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 0.5 hour and the temperature was allowed to rise to room temperature. A saturated solution of ammonium chloride (150 ml) was added cautiously and the layers were separated. The organic extract was washed with water (2×50 ml) hydrochloric acid (2M, 2×50 ml) and water (2×50 ml). The solution was dried (anhydrous sodium sulphate) and filtered. The filtrate was evaporated to dryness and the residue was distilled to give t-butyl 3-(1-ethoxycarbonylcyclopropyl)-3-oxopropionate (11.66 g) as a clear oil bp 89°-90° C./0.5 mmHg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05859283
출처 데이터셋uspto-grants-1999_01
ORD IDord-f9dec02b51f04427a9068269433814fd
출처 메모uspto-grants-1999_01