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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264469생성일: 2026년 10월 26일

Sodium Chloride → Rac-6-methoxy-2-(3-oxo-2-butyl)-1-indanone

https://huagongshe.com/reaction/264469

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물DiisopropylamineHCID 7912—
반응물TetrahydrofuranHCID 8028—
반응물6-Methoxy-1-IndanoneHCID 334036—
반응물Lithium diisopropylamideHCID 2724682—
반응물ButyllithiumHCID 178418339—
용매HexaneHCID 8058—
생성물Rac-6-methoxy-2-(3-oxo-2-butyl)-1-indanoneHCID 5368761037%

반응 단계

A lithium diisopropylamide solution, freshly prepared from 3.12 ml of diisopropylamine and 13.8 ml of 1.6N n-butyllithium in hexane, in 40 ml of anhydrous tetrahydrofuran was added dropwise while stirring to a solution, cooled to -70°, of 2.96 g of 6-methoxy-1-indanone in 300 ml of anhydrous tetrahydrofuran. The mixture was stirred at this temperature for an additional 30 minutes and a solution of 2.03 ml of 3-chloro-2-butenone dissolved in 40 ml of anhydrous tetrahydrofuran was subsequently added dropwise over 10 minutes. The reaction mixture was left to come to room temperature over 30 minutes and was stirred at this temperature for a further 30 minutes. Subsequently, the reaction mixture was poured on to 150 ml of ice, 150 ml of saturated sodium chloride were added and the organic phase was separated. The aqueous phase was extracted once with 400 ml of diethyl ether, the combined organic phases were washed once with 200 ml of saturated sodium chloride solution, dried over magnesium sulfate and concentrated in a vacuum. The red oil obtained was purified by column chromatography on silica gel (hexane/diethyl ether 3:2). In addition to 0.93 g of educt there were obtained 1.56 g (37%) of rac-6-methoxy-2-(3-oxo-2-butyl)-1-indanone as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646173
출처 데이터셋uspto-grants-1997_07
ORD IDord-f7f39915f30143158627a1f5c5da9543
출처 메모uspto-grants-1997_07