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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1522706생성일: 2026년 10월 25일

Toluene → 5-Methyl-2-phenylpyridine

https://huagongshe.com/reaction/1522706

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Phenylboronic AcidHCID 66827—
반응물2-Bromo-5-methylpyridineHCID 564216—
촉매Tris(dibenzylideneacetone) dipalladiumHCID 9832798—
촉매2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
용매WaterHCID 962—
생성물5-Methyl-2-phenylpyridineHCID 4746792%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09076973B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-c839b2803eb649b180725a3fe95a315a
출처 메모uspto-grants-2015_07