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HRID 29456作成日:2026年10月26日

1-methyl-1H-1,3-benzodiazole-2-carbaldehyde → (1-methyl-1H-1,3-benzodiazol-2-yl)methanol

https://huagongshe.com/reaction/29456

反応式

関与物質

役割名称HCID仕込み量
反応物1-methyl-1H-1,3-benzodiazole-2-carbaldehydeHCID 762084—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物(1-methyl-1H-1,3-benzodiazol-2-yl)methanolHCID 344177—

反応手順

To 432 mg of 1-methyl-1H-benzoimidazole-2-carbaldehyde (2.7 mmol, 1 eq) dissolved in a mixture of THF (10 mL) and methanol (10 mL) was added 340 mg of sodium borohydride (9.0 mmol, 3.33 eq) in several portions. After 12 h the reaction mixture was quenched with water and extracted with ethyl acetate. The organics were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to give (1-methyl-1H-benzoimidazol-2-yl)-methanol in quantitative yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.8 (s, 3 H) 4.7 (d, J=5.6 Hz, 2 H) 5.6 (t, J=5.7 Hz, 1 H) 7.2 (m, 1 H) 7.2 (m, 1 H) 7.5 (m, 1 H) 7.6 (m, 1 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420001B2
出典データセットuspto-grants-2008_09
ORD IDord-0ad2e10d90d74c3faa56969db1eb728f
出典メモuspto-grants-2008_09