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HRID 2108035作成日:2026年10月26日

Acetic Acid → 5-Bromo-2-pyridinepropanol

https://huagongshe.com/reaction/2108035

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3-(5-Bromopyridin-2-yl)prop-2-yn-1-olHCID 13979730—
溶媒PyridineHCID 1049—
生成物5-Bromo-2-pyridinepropanolHCID 1397973582.4%

反応手順

To a suspension of 3-(5-bromo-2-pyridinyl)-2-propyn-1-ol (0.5 g) and dipotassium azadicarboxylate (3.66 g) in pyridine (40 ml) was added acetic acid (2 ml) and the mixture stirred at room temperature for 24 h, with further additions of acetic acid after 2 h (0.16 ml) and 17 h (2.16 ml). As reduction had only partially gone to completion, further dipotassium azadicarboxylate (3.2 g) and acetic acid (1.86 ml) were added, and stirring continued for 17 h. The mixture was quenched with water (15 ml) and evaporated in vacuo. The residue was co-evaporated with toluene (15 ml) and the residue partitioned between 8% sodium bicarbonate solution (60 ml) and ethyl acetate (60 ml) and the organic phase dried and evaporated in vacuo. The oily residue was purified by FCC using ether and ether-methanol (5%) eluants to afford the title compound as a yellow oil (0.42 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04937251
出典データセットuspto-grants-1990_06
ORD IDord-65d6daa4aa4342ff8a2038e551438cdb
出典メモuspto-grants-1990_06