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HRID 2117682생성일: 2026년 10월 25일

Diethyl Ether → 1-Bromo-7-(prop-2-yn-1-yloxy)heptane

https://huagongshe.com/reaction/2117682

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Propargyl alcoholHCID 7859—
반응물Sodium HydroxideHCID 14798—
반응물1,7-DibromoheptaneHCID 78309—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
생성물1-Bromo-7-(prop-2-yn-1-yloxy)heptaneHCID 2189554017%

반응 조건

온도60 °C

반응 단계

25% (w/w) aq. NaOH (700 ml) was added to a stirred mixture of propargyl alcohol (70 g), tetra-butyl ammonium bromide (3.5 g) and 1,7-dibromoheptane (322 g) maintaining the temperature below 30° C. The reaction mixture was heated at 60° C. for 5 hrs then allowed to cool to room temperature and stirred overnight. Diethyl ether (350 ml) and water (280 ml) were added, the mixture stirred and allowed to settle. The aqueous layer was extracted with diethyl ether (210 ml), the organic layers combined, dried (MgSO4). The solution was concentrated to give 280 g of crude material. 140 g Of the crude was purified by chromatography on Biotage (800 g) eluting with petroleum ether then petroleum ether:ethyl acetate (100:1 followed by 100:1.5) to give the title compound (49.6 g). NMR—300 MHz—δ (CDCl3)—4.05 (2H, d, J 2 Hz), 3.45 (2H, t, J 6.5 Hz), 3.35 (2H, t, J 7 Hz), 2.35 (1H, s), 1.8 (2H, m), 1.5 (2H, m), 1.3 (4H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07442719B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-928972620f544a12a2876e271dcbf73e
출처 메모uspto-grants-2008_10