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HRID 2779作成日:2026年10月23日

5-Bromo-2-fluorobenzaldehyde → (5-Bromo-2-fluorophenyl)methanol

https://huagongshe.com/ja/reaction/2779

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-2-fluorobenzaldehydeHCID 736327—
反応物Sodium borohydrideHCID 4311764—
溶媒TetrahydrofuranHCID 8028—
生成物(5-Bromo-2-fluorophenyl)methanolHCID 277335297.7%

反応条件

温度0 °C

反応手順

To a solution of 5-bromo-2-fluoro-benzaldehyde (6.10 g, 30.0 mmol) in 30 mL of THF at 0° C. is added 5 mL of sodium borohydride (2.0M solution in triglyme, 10.0 mmol). The reaction mixture is stirred at 0° C. for 25 min and then quenched by the addition of 1N HCl. The mixture is diluted with EtOAc and the layers are separated. The organic layer is washed with H2O and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with 15% EtOAc/hexanes to afford the title compound (6.00 g, 29.3 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731315
出典データセットuspto-grants-1998_03
ORD IDord-dfa8e518af0e4946b9f86e5f4d0e8666
出典メモuspto-grants-1998_03