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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1089255생성일: 2026년 10월 24일

2-Butene-1,4-diol → 1,4-Bis(4-methoxybenzyloxy)but-2-ene

https://huagongshe.com/ko/reaction/1089255

반응식

참여 물질

역할이름HCID투입량
반응물2-Butene-1,4-diolHCID 8065—
반응물Sodium hydrideHCID 24758—
반응물4-Methyloxybenzyl chlorideHCID 69993—
용매DimethylformamideHCID 6228—
생성물1,4-Bis(4-methoxybenzyloxy)but-2-eneHCID 5455513770%

반응 단계

To a solution of 2-buten-1,4-diol (4.9 g, 60 mmol) in dry dimethylformamide (120 ml) was added sodium hydride (60% dispersion in oil; 5.28 g, 132 mmol) and the mixture was stirred at room temperature for 100 minutes. To this solution was added 4-methoxybenzyl chloride (17.9 ml, 132 mmol) in dimethylformamide (30 ml) dropwise over 45 minutes and the mixture was stirred for a further 40 minutes. The mixture was partitioned between ether (150 ml) and water (150 ml). The organic layer was further washed with water (150 ml), dried (magnesium sulphate) and the solvent was removed. The residue was purified by column chromatography on silica gel eluting with hexane-acetone (4:1, 3:1) to afford 1,4-bis(4-methoxybenzyloxy)but-2-ene as a clear colourless liquid (13.7 g, 70%). IR: υmax (film) 2840, 1615, 1515 and 1250 cm-1. 1H NMR: δH (CDCl3) 3.80 (6H, s, 2×CH3), 4.02 (4H, d, J=4.5 Hz, 2×CHCH2), 4.43 (4H, s, 2×ArCH2), 5.79 (2H, t, J=4.5 Hz, 2×CH), 6.88 (4H, d, J=9 Hz, ArH) and 7.27 (4H, d, J=9 Hz, ArH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04965270
출처 데이터셋uspto-grants-1990_10
ORD IDord-7012a792d1d44d4a9d86aaa7bc5c10f1
출처 메모uspto-grants-1990_10