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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1066896생성일: 2026년 10월 26일

5-Bromo-2-methoxybenzaldehyde → HCID 19379069, 화합물

https://huagongshe.com/reaction/1066896

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참여 물질

역할이름HCID투입량
반응물5-Bromo-2-methoxybenzaldehydeHCID 90684—
반응물Cyclopentyltriphenylphosphonium bromideHCID 2735896—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물HCID 19379069HCID 1937906984.5%

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온도0 °C

반응 단계

n-BuLi (1.6M solution in hexane) (72.5 ml, 116 mmol) was added dropwise at 0° C. to a solution of cyclopentyltriphenylphosphonium bromide (45.8 g, 111 mmol) in THF (300 ml). The red solution was stirred at 0° C. for 0.5 h then treated with a solution of 5-bromo-2-methoxybenzaldehyde (23.5 g, 109 mmol) in THF (150 ml). The reaction mixture was stirred at RT overnight, concentrated in vacuo, then partitioned between CH2Cl2 (250 ml) and water (150 ml). The organic phase was separated and combined with further CH2Cl2 extracts (2×50 ml). The organic phase was washed (brine; 50 ml), dried (Na2SO4), and concentrated in vacuo. The residue was subjected to chromatography (SiO2; CH2Cl2) to afford the title compound (24.6 g), as a colourless oil δH (80 MHz; CDCl3) 1.6-1.9 (4H, br m, CH2(CH2)2), 2.3-2.6 (4H, br m, CH2(CH2)2CH2), 3.76 (3H, s, OMe), 6.4-6.5 (1H, br m, CH═C), 6.65 (1H, d, J 8.5 Hz, ArH ortho to OMe), 7.18 (1H, dd, J 8.5, 2.4 Hz, ArH para to olefin), and 7.39 (1H, d, J 2.4 Hz, ArH ortho to olefin).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06245774B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-983e9cea9e384e9c8b092cbe776e7a7e
출처 메모uspto-grants-2001_06