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HRID 7151作成日:2026年10月23日

Borane;tetrahydrofuran → (3-Ethoxypyridin-2-yl)methanol

https://huagongshe.com/ja/reaction/7151

反応式

関与物質

役割名称HCID仕込み量
反応物Borane;tetrahydrofuranHCID 2723981—
反応物3-Ethoxypyridine-2-carboxylic acidHCID 21333204—
溶媒TetrahydrofuranHCID 8028—
生成物(3-Ethoxypyridin-2-yl)methanolHCID 22018715124.6%

反応手順

To a solution of 3-ethoxypicolinic acid (0.202 g, 1.21 mmol) in dry THF (1 mL) was added BH3.THF (1.0 M in THF, 5.0 mL, 5.0 mmol) and the reaction mixture stirred at room temperature for 2.5 hours. The mixture was then quenched with methanol (20 mL), stirred at reflux for 4 hours and concentrated under reduced pressure. The resultant crude product was dissolved in methanol (3×15 mL) and concentrated to give the desired crude alcohol (0.231 g) as an orange solid. 1H NMR (CDCl3): δ 1.46 (t, 3H, J=7.0 Hz), 4.07 (q, 2H, J=7.0 Hz), 4.74 (s, 2H), 7.09–7.20 (m, 2H), 8.14 (d, 1H, J=4.5 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084155B2
出典データセットuspto-grants-2006_08
ORD IDord-ccee693cbf364a5ab48c75de7b438da3
出典メモuspto-grants-2006_08