戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 471567作成日:2026年10月25日

Potassium Carbonate → (E)-2-amino-6-(3-methoxyprop-1-enyl)benzonitrile

https://huagongshe.com/reaction/471567

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-Amino-6-bromobenzonitrileHCID 9813038—
反応物2-[(1E)-3-methoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 16217443—
触媒HCID 178418397HCID 178418397—
溶媒Ethyl AcetateHCID 8857—
溶媒Water 1,2-dimethoxyethaneHCID 18180031—
生成物(E)-2-amino-6-(3-methoxyprop-1-enyl)benzonitrileHCID 67399559—

反応条件

温度85 °C

反応手順

To a solution of 2-amino-6-bromobenzonitrile (1.0 g, 5.0 mmol), (E)-2-(3-methoxypropenyl)-4,4,5,5-tetramethyl-(1,3,2)-dioxaboroane (1.2 g, 6.0 mmol), and K2CO3 (1.38 g, 10.0 mmol) in DME/H2O (4:1, 20 mL) was added Pd(PPh3)4 (289 mg) at room temperature under nitrogen. The reaction mixture was warmed to 85° C. and stirred at that temperature under nitrogen overnight. After it was cooled down to room temperature, the reaction solution was diluted with EtOAc, washed with brine (2×), and dried over Na2SO4. After removal of the solvent, the residue was purified by chromatography on silica gel eluting with 30% EtOAc in hexanes to give the title compound as a pale-yellow solid. 1H NMR (400 MHz, CDCl3) δ 3.40 (s, 3H), 4.12 (dd, J=6.0, 1.8 Hz, 2H), 4.42 (s, 2H), 6.42 (dt, J=16.0, 5.8 Hz, 1H), 6.63 (d, J=8.0 Hz, 1H), 6.85 (d, J=16.0 Hz, 1H), 6.93 (d, J=8.0 Hz, 1H), 7.26 (t, J=8.0 Hz, 1H). 13C NMR (CDCl3) δ 58.2, 72.7, 95.4, 113.6, 115.0, 116.6, 128.5, 130.9, 133.4, 140.3, 150.1. MS 189 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633186B2
出典データセットuspto-grants-2014_01
ORD IDord-e599497e7754404186210a19c2f23962
出典メモuspto-grants-2014_01