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HRID 1900524생성일: 2026년 10월 25일

Ammonium Chloride → 5-Acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuran

https://huagongshe.com/reaction/1900524

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Heptyltriphenylphosphonium bromideHCID 2724567—
반응물5-Acetoxy-4,6-di-tert-butyl-2-formylbenzofuranHCID 22918669—
반응물ButyllithiumHCID 178418339—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물5-Acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuranHCID 5376872197%

반응 단계

A pentane solution (6.0 ml) of 1.6M n-butyllithium was added dropwise to a solution of n-heptyltriphenylphosphonium bromide (4.2 g) in tetrahydrofuran (30 ml) under a nitrogen atmosphere. After stirring the mixture at room temperature for 90 min, a solution of 5-acetoxy-4,6-di-tert-butyl-2-formylbenzofuran (2.54 g) in tetrahydrofuran (20 ml) was added dropwise. Subsequently, the mixture was heated under reflux for 1 h and, after cooling, a saturated aqueous solution of ammonium chloride was added and the mixture was subjected to extraction with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 5-acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuran [3.1 g (yield, 97%)] as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05574178
출처 데이터셋uspto-grants-1996_11
ORD IDord-6caa1f97d57148d39032603748e39bcd
출처 메모uspto-grants-1996_11