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HRID 2117682作成日:2026年10月26日

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

https://huagongshe.com/reaction/2117682

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Propargyl alcoholHCID 7859—
反応物Sodium HydroxideHCID 14798—
反応物1,7-DibromoheptaneHCID 78309—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
生成物1-Bromo-7-(prop-2-yn-1-yloxy)heptaneHCID 2189554017%

反応条件

温度60 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07442719B2
出典データセットuspto-grants-2008_10
ORD IDord-928972620f544a12a2876e271dcbf73e
出典メモuspto-grants-2008_10