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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 981139생성일: 2026년 10월 25일

Water → (E)-4-[3-Methoxy-4-(methoxymethoxy)phenyl]-3-buten-1-ol

https://huagongshe.com/reaction/981139

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-Methoxy-4-(methoxymethoxy)benzaldehydeHCID 79661—
반응물Phosphonium, (3-hydroxypropyl)triphenyl-, bromideHCID 11025793—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(E)-4-[3-Methoxy-4-(methoxymethoxy)phenyl]-3-buten-1-olHCID 2007144735.5%

반응 단계

n-Butyllithium (1.6 M in hexane, 25 ml) was added dropwise to a stirred suspension of (3-hydroxypropyl)triphenylphosphonium bromide (8.03 g) in dry THF (50 ml) cooled to 0° under nitrogen. The resulting blood-red solution was stirred at 0° for 10 min and then 3methoxy-4-(methoxymethoxy)benzaldehyde (3.60 g) in dry THF (10 ml) was added dropwise over 5 min. The mixture was allowed to warm to room temperature, stirred for 4 h water (10 ml) was added and the majority of the solvent was removed in vacuo at 40°. A solution of the residual oil in ER (200 ml) was washed with water (150 ml), dried, treated with charcoal, concentrated and purified by [FCS] eluting with EA/hexane (1:1) to give the title compound (1.55 g). T.l.c. (EA-hexane 1:1) Rf 0.30.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04990505
출처 데이터셋uspto-grants-1991_02
ORD IDord-4aa5abc2b64446508fa58debd6b181ef
출처 메모uspto-grants-1991_02