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HRID 1066896作成日:2026年10月27日

5-Bromo-2-methoxybenzaldehyde → HCID 19379069、化合物

https://huagongshe.com/reaction/1066896

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-2-methoxybenzaldehydeHCID 90684—
反応物Cyclopentyltriphenylphosphonium bromideHCID 2735896—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 19379069HCID 1937906984.5%

反応条件

温度0 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06245774B1
出典データセットuspto-grants-2001_06
ORD IDord-983e9cea9e384e9c8b092cbe776e7a7e
出典メモuspto-grants-2001_06