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HRID 54591作成日:2026年10月24日

Bromocyclopentane → 3-Cyclopentyloxy-4-methoxybenzaldehyde

https://huagongshe.com/ja/reaction/54591

反応式

関与物質

役割名称HCID仕込み量
反応物BromocyclopentaneHCID 8728—
反応物Cesium carbonateHCID 10796—
反応物IsovanillinHCID 12127—
溶媒DimethylformamideHCID 6228—
生成物3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 273589389.4%

反応手順

Cs2CO3 (214 g, 0.66 mol) was added to a mixture of 3-hydroxy-4-methoxybenzaldehyde (100 g, 0.66 mol) and cyclopentyl bromide (98 g, 0.66 mol) in anhydrous DMF (500 ml). The reaction mixture was stirred at RT for 16 h, then treated with a further portion of cyclopentyl bromide (98 g, 0.66 mol) and CS2CO3 (214 g, 0.66 mol). After a further 6h at RT, the mixture was filtered and concentrated in vacuo. The residue was dissolved in CH2Cl2 (300 ml) and washed with NaOH solution (10%, 2×150 ml). The organic layer was dried (MgSO4), concentrated in vacuo, and distilled (150° C., 10-2 mbar) to afford the title compound (130 g) as a viscous colorless oil. δH (CDCl3) 1.5-2.0 (8H, br m, CH2)4), 3.87 (3H, s, OCH3), 4.80 (1H, br m, OCHCH2), 6.90 (1H, d, J 8.7 Hz, ArH ortho to OMe), 7.30-7.45 (2H, m, 2×ArH meta to OMe), and 9.77 (1H, s, ArCHO).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622977
出典データセットuspto-grants-1997_04
ORD IDord-25e19a8ecbfe48e2aab63a4bb4fc0483
出典メモuspto-grants-1997_04