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HRID 1798709作成日:2026年10月27日

Methyl 5-methylpicolinate → (5-Methylpyridin-2-yl)methanol

https://huagongshe.com/reaction/1798709

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 5-methylpicolinateHCID 268759—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物(5-Methylpyridin-2-yl)methanolHCID 1232538772.9%

反応手順

Sodium borohydride (4.5 g, 115. mmol) was added to a solution of methyl 5-methylpicolinate (6.0 g, 39.5 mmol) in THF (60 mL) and methanol (6 ml) at RT. The reaction mixture was stirred at RT for 2 h (the reaction was monitored by TLC). The mixture was concentrated under reduced pressure and the residue was diluted with water and extracted with EtOAc. The combined organics were dried over sodium sulfate, filtered and concentrated under reduced pressure. The organic layer was concentrated under vacuo to afford (5-methylpyridin-2-yl)methanol (3.5 g, 72.9%) as an off-white solid. 1H NMR: 200 MHz, CDCl3: δ 8.5 (s, 1H), 7.7 (d, 1H), 7.15 (d, 1H), 5.0 (s, 3H), 3.4 (s, 3H). MS: [M+H]+: m/z=124.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08343973B2
出典データセットuspto-grants-2013_01
ORD IDord-225c87e4b9234500abbf9627801447ba
出典メモuspto-grants-2013_01