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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 918생성일: 2026년 10월 23일

Bromocyclopentane → 3-Cyclopentyloxy-4-methoxybenzaldehyde

https://huagongshe.com/ko/reaction/918

반응식

참여 물질

역할이름HCID투입량
반응물BromocyclopentaneHCID 8728—
반응물Cesium carbonateHCID 10796—
반응물IsovanillinHCID 12127—
용매DimethylformamideHCID 6228—
생성물3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 273589389.4%

반응 단계

Caesium carbonate (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 (50 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 caesium carbonate (214 g, 0.66 mol). After a further 6 h at RT, the mixture was filtered and concentrated in vacuo. The residue was dissolved in dichloromethane (300 ml) and washed with sodium hydroxide 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 colourless oil. (Found: C, 70.38; H, 7.48. C13H16O3 requires C, 70.89; H 7.32%); δH (CDCl3) 1.5-2.0 (8H, br m, CH2)4), 3.87 (3H, s, OMe), 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 (1 H, s, ArCHO).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723460
출처 데이터셋uspto-grants-1998_03
ORD IDord-8d66976050a242adaad6949712ee0b51
출처 메모uspto-grants-1998_03