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HRID 712472作成日:2026年10月24日

Benzyl Bromide → (3-(Benzyloxy)pyridin-2-yl)methanol

https://huagongshe.com/ja/reaction/712472

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium HydroxideHCID 14797—
反応物3-Hydroxypyridine-2-methanolHCID 84169—
溶媒EthanolHCID 702—
生成物(3-(Benzyloxy)pyridin-2-yl)methanolHCID 1321754065%

反応手順

To a solution of 3-hydroxy-2-(hydroxymethyl)pyridine (10.00 g) and KOH (7.00 g) in anhydrous EtOH was added benzyl bromide (7.30 mL) at room temperature under stirring. The reaction mixture was heated to reflux for 24 h, then cooled to rt and filtered. The filtrate was concentrated in vacuo and the residue was chromatographed with a silica gel column (eluting agent: 20:1 (v/v) DCM/MeOH) to give the title compound as a pale yellow solid (7.50 g, 65.00%), HPLC: 95.00%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 216.4 (M+1); 1H NMR (400 MHz, CDCl3) δ: 4.39 (br s, 1H), 4.82 (s, 2H), 5.11 (s, 2H), 7.16-7.17 (m, 2H), 7.34-7.40 (m, 5H), 8.15-8.17 (m, 1H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181277B2
出典データセットuspto-grants-2015_11
ORD IDord-7452e675d20641e6b0762bc342aefbf1
出典メモuspto-grants-2015_11