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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 718553생성일: 2026년 10월 25일

Water → 5-(4-(3-Isopropylphenyl)pent-1-enyl)benzo[d][1,3]dioxole

https://huagongshe.com/reaction/718553

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물FlorhydralHCID 86209—
반응물(Benzo[d][1,3]dioxol-5-ylmethyl)triphenylphosphonium bromideHCID 10695955—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물5-(4-(3-Isopropylphenyl)pent-1-enyl)benzo[d][1,3]dioxoleHCID 6798293776.2%

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온도0 °C

반응 단계

A solution of (benzo[d][1,3]dioxol-5-ylmethyl)triphenylphosphonium bromide (4.77 g, 10.0 mmol, 1.0 equiv.) in THF (20 mL), was cooled to 0° C. After adding n-BuLi (1.6 M in hexanes, 6.3 mL, 10.0 mmol, 1.0 equiv.) at 0° C., the dark red suspension was stirred at 0° C. for 10 min. 3-(3-Isopropylphenyl)butanal (1.90 g, 10.0 mmol, 1.0 equiv.) in THF (10 mL) was added, and the mixture was stirred at 0° C.→25° C. for 16 h. After addition of H2O at 25° C., the aqueous layer was extracted with hexanes and MTBE, the combined organic phases were dried (MgSO4), filtered and the filtrate was concentrated. The residue was purified by flash chromatography on SiO2 (hexanes/EtOAc 4:1) to yield 2.35 g (75%) of the title compound as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09193935B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-9d733e36c8b14f94b8fe3ac8e3578bca
출처 메모uspto-grants-2015_11