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HRID 1297004作成日:2026年10月25日

Benzene, 2-bromo-1,4-dimethyl- → 2,5-Dimethylbiphenyl

https://huagongshe.com/reaction/1297004

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 2-bromo-1,4-dimethyl-HCID 11121—
反応物Phenylboronic AcidHCID 66827—
反応物Potassium FluorideHCID 522689—
触媒palladium(II) acetateHCID 167845—
触媒2-(Di-tert-butylphosphino)biphenylHCID 2734215—
溶媒TetrahydrofuranHCID 8028—
生成物2,5-DimethylbiphenylHCID 52250682%

反応手順

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 2-bromo-p-xylene (0.138 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 149 mg (82%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07247731B2
出典データセットuspto-grants-2007_07
ORD IDord-ce6271a8c2344a96b3678ec12c1bd254
出典メモuspto-grants-2007_07