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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264472생성일: 2026년 10월 25일

Sodium Chloride → (RS)-6-methoxy-2-(2-oxopropyl)-1-indanone

https://huagongshe.com/reaction/264472

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물ChloroacetoneHCID 6571—
반응물DiisopropylamineHCID 7912—
반응물6-Methoxy-1-IndanoneHCID 334036—
반응물Lithium diisopropylamideHCID 2724682—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물(RS)-6-methoxy-2-(2-oxopropyl)-1-indanoneHCID 1903638156%

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 1.62 ml of chloroacetone 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 90 minutes and was stirred at this temperature for an additional 45 minutes. Subsequently, the reaction mixture was poured on to 100 ml of ice, 100 ml of saturated sodium chloride were added and the organic phase was separated. The aqueous phase was extracted once with 300 ml of diethyl ether. The combined organic phases were washed once with 100 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). There were obtained 2.24 g (56%) of (RS)-6-methoxy-2-(2-oxopropyl)-1-indanone as a yellow solid which was used without further recrystallization in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646173
출처 데이터셋uspto-grants-1997_07
ORD IDord-81a06cb0d0f244de9a1166de4f0721bc
출처 메모uspto-grants-1997_07