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HRID 708306作成日:2026年10月25日

Thiophene, 2,3,5-tribromo- → 3-Bromo-2,5-bis(4-(tert-butyl)phenyl)thiophene

https://huagongshe.com/reaction/708306

反応式

関与物質

役割名称HCID仕込み量
反応物Thiophene, 2,3,5-tribromo-HCID 76592—
反応物4-tert-Butylphenylboronic acidHCID 2734320—
反応物Sodium Carbonate MonohydrateHCID 2735133—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-Bromo-2,5-bis(4-(tert-butyl)phenyl)thiopheneHCID 6797358389%

反応手順

Sodium carbonate monohydrate (58.0 g, 468 mmol) was dissolved in water (500 mL) and a solution of 4-(tert-butyl)-phenylboronic acid (40.0 g) and 2,3,5-tribromothiophene (30.0 g, 94 mmol) in THF (500 mL) was added, and deoxygenated by bubbling with argon. Pd(PPh3)4 (5.0 g, 4.30 mmol) was added and the mixture refluxed for 24 h. The mixture was cooled and the aqueous phase separated and extracted with EtOAc. Organic fractions were combined washed with water (500 mL) and dried over MgSO4. The solvent was evaporated and the crude product washed in MeOH, filtered and dried overnight to afford a light yellow, powdery solid (35.46 g, 89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09176357B2
出典データセットuspto-grants-2015_11
ORD IDord-1995a93b609848b0a366d2f4f7a5bf92
出典メモuspto-grants-2015_11