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HRID 1919481作成日:2026年10月26日

Methanol → (4-Bromo-2,5-difluorophenyl)methanol

https://huagongshe.com/reaction/1919481

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物4-Bromo-2,5-difluorobenzoic acidHCID 822857—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Bromo-2,5-difluorophenyl)methanolHCID 5340141885%

反応手順

To a solution of 2 g (8.44 mmol) of 4-bromo-2,5-difluorobenzoic acid (prepared according to the procedure of Ishikawa et al., Kogyo Kagaku Zasshi, pg 972-979, 1970) in 20 mL of tetrahydrofuran was added 40 mL of a 1M solution of borane-tetrahydrofuran complex. The solution was heated under reflux for 64 h, cooled to ambient temperature and 100 mL of methanol was added. The reaction was then heated for a further 2 h, cooled and concentrated in vacuo. Purification by flash chromatography (silica gel, 9:1 hexane:ethyl acetate) afforded 1.6 g of 4-bromo-2,5-difluorobenzyl alcohol. To a solution of 1.3 g (5.6 mmol) of 4-bromo-2,5-difluorobenzyl alcohol in 20 mL of dichloromethane at 0° C. was added 2.27 g (6.7 mmol) of carbon tetrabromide and 1.8 g (6.7 mmol) of triphenylphosphine. The reaction was stirred for 2 h at this temperature, the solvent was removed in vacuo and the residue stirred with 100 mL of diethyl ether. The solution was filtered, concentrated in vacuo, and purified by flash chromatography (silica gel, 9:1 hexane:ethyl acetate) to afford 1.5 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08168637B2
出典データセットuspto-grants-2012_05
ORD IDord-47b3495e0c2e4f5a909f9a70e388e40b
出典メモuspto-grants-2012_05