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HRID 1522706作成日:2026年10月26日

Toluene → 5-Methyl-2-phenylpyridine

https://huagongshe.com/reaction/1522706

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Phenylboronic AcidHCID 66827—
反応物2-Bromo-5-methylpyridineHCID 564216—
触媒Tris(dibenzylideneacetone) dipalladiumHCID 9832798—
触媒2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
溶媒WaterHCID 962—
生成物5-Methyl-2-phenylpyridineHCID 4746792%

反応手順

2-bromo-5-methylpyridine (11.25 g, 65.39 mmol), phenylboronic acid (9.5 g, 78.47 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (1.0 g, 2.61 mmol), and potassium phosphate tribasic (45 g, 196.17 mmol), 250 mL of toluene and 25 mL of water were placed in a 500 mL round-bottom flask. Nitrogen was bubbled directly into the mixture for 30 min after which tris(dibenzylideneacetone) dipalladium(0) (598 mg, 0.653 mmol) was added. Nitrogen was bubbled for another 15 min then the reaction mixture was heated to reflux for 16 h under nitrogen. The mixture was cooled and the organic layer was separated from the aqueous layer. The organic layers are washed with saturated brine solution, dried over magnesium sulfate, filtered, and the solvent removed under vacuum to give an off-white solid as the crude. The crude was purified by column chromatography using silica gel as the stationary phase and 5%-10% ethyl acetate in hexanes as the mobile phase. 10.11 g of desired product was obtained after purification (92% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09076973B2
出典データセットuspto-grants-2015_07
ORD IDord-c839b2803eb649b180725a3fe95a315a
出典メモuspto-grants-2015_07