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HRID 1190989作成日:2026年10月26日

Dichloromethane → (E)-5-(2-Cyclohexylvinyl)-pyridine-2-carbonitrile

https://huagongshe.com/reaction/1190989

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Sodium CarbonateHCID 10340—
反応物5-Bromopyridine-2-carbonitrileHCID 817154—
反応物2-Cyclohexylvinyl boronic acidHCID 4185149—
溶媒1,4-DioxaneHCID 31275—
生成物(E)-5-(2-Cyclohexylvinyl)-pyridine-2-carbonitrileHCID 5849546576%

反応条件

温度90 °C

反応手順

Combine a mixture of 5-bromo-2-cyano-pyridine (2 g, 10.93 mmol), 2-cyclohexylvinyl boronic acid (2.52 g, 16.39 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with DCM (446 mg, 0.546 mmol) and 2M aqueous Na2CO3 (18.2 mL, 36.07 mmol) in 1,4-dioxane (110 mL). Purge with nitrogen and heat at 90° C. overnight. Cool the reaction to room temperature and partition between EtOAc and water. Separate the aqueous phase and extract with EtOAc. Dry the combined organic extracts over MgSO4, filter and concentrate in vacuo. Purify by chromatography on silica gel (120 g, pre-packed cartridge) eluting stepwise with hexane/EtOAc (1:0 over 5 min, 49:1 over 5 min and 19:1 over 5 min; 50 mL/min) to obtain the desired intermediate (1.76 g, 76%). MS (APCI+) m/z: 213 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08680091B2
出典データセットuspto-grants-2014_03
ORD IDord-01ff898b45c445bcab9f091c7aabacf8
出典メモuspto-grants-2014_03