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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1376967생성일: 2026년 10월 26일

Pentane → 5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuran

https://huagongshe.com/reaction/1376967

반응식

참여 물질

역할이름HCID투입량
반응물PentaneHCID 8003—
반응물Heptyltriphenylphosphonium bromideHCID 2724567—
반응물5-Benzyloxy-4-t-butyl-2-formylbenzofuranHCID 23442879—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuranHCID 5430872291.2%

반응 단계

A pentane solution (2.6 ml, 4.2 mmol) of 1.6M n-butyllithium was added dropwise to a solution of n-heptyltriphenylphosphonium bromide (1.84 g, 4.2 mmol) in tetrahydrofuran (10 ml) under a nitrogen atmosphere. After stirring the mixture at room temperature for 30 min, a solution of 5-benzyloxy-4-tert-butyl-2-formylbenzofuran (1.0 g, 3.2 mmol) in tetrahydrofuran (10 ml) was added dropwise. Subsequently, the mixture was stirred at room temperature for 30 min, poured into ice water and subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and water, then dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica Gel chromatography (chloroform) to afford 5-benzyloxy-4-tert-butyl-2-(1-octenyl)benzofuran [1.14 g (yield, 91%)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05663373
출처 데이터셋uspto-grants-1997_09
ORD IDord-8f9839940081438eb9ea5381c16840c8
출처 메모uspto-grants-1997_09