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HRID 1919482作成日:2026年10月26日

Carbon tetrabromide → 1-Bromo-4-(bromomethyl)-2,5-difluorobenzene

https://huagongshe.com/reaction/1919482

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon tetrabromideHCID 11205—
反応物TriphenylphosphineHCID 11776—
反応物(4-Bromo-2,5-difluorophenyl)methanolHCID 53401418—
溶媒DichloromethaneHCID 6344—
生成物1-Bromo-4-(bromomethyl)-2,5-difluorobenzeneHCID 2191121093.7%

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-41d424f9ea144483a9aac952414d7119
出典メモuspto-grants-2012_05