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HRID 390328作成日:2026年10月24日

Sodium Hydroxide → 2-(Diphenylmethyleneamino)-3-(4-fluorophenyl)propanenitrile

https://huagongshe.com/ja/reaction/390328

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物4-Fluorobenzyl bromideHCID 68021—
反応物[(Diphenylmethylene)amino]acetonitrileHCID 612957—
触媒Benzyltrimethylammonium chlorideHCID 5963—
溶媒DichloromethaneHCID 6344—
生成物2-(Diphenylmethyleneamino)-3-(4-fluorophenyl)propanenitrileHCID 5845891092%

反応手順

To a solution of 2-(diphenylmethyleneamino)acetonitrile (1.21 g, 5.47 mmol, 1.0 equiv) in CH2Cl2 (9.12 mL) was added 4-fluorobenzyl bromide (0.75 mL, 6.02 mmol, 1.1 equiv), benzyltrimethylammonium chloride (0.10 g, 0.547 mmol, 0.1 equiv), and NaOH (0.99 mL of a 10 M aqueous solution, 9.85 mmol, 1.8 equiv). The reaction was stirred vigorously for 18 h, at which time TLC analysis indicated complete consumption of the starting nitrile. The reaction was added to water and extracted with CH2Cl2 (×3). The combined CH2Cl2 extracts were dried (Na2SO4) and concentrated in vacuo. The crude product was purified by silica gel chromatography (5-30% ethyl acetate/hexane) to provide the title compound (1.65 g, 92% yield) as a viscous yellow oil. 1H NMR (400 MHz, CDCl3) δ ppm 7.54-7.65 (m, 2H), 7.38-7.48 (m, 4H), 7.31-7.38 (m, 2H), 7.00-7.09 (m, 2H), 6.89-6.97 (m, 2H), 6.84 (d, J=6.30 Hz, 2H), 4.35 (dd, J=7.81, 6.04 Hz, 1H), 3.10-3.29 (m, 2H); LCMS (ES+, (M+H)+) m/z 329.25.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383639B2
出典データセットuspto-grants-2013_02
ORD IDord-bcd505dce2a9457487636a9990a7264e
出典メモuspto-grants-2013_02