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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390328생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물4-Fluorobenzyl bromideHCID 68021—
반응물[(Diphenylmethylene)amino]acetonitrileHCID 612957—
촉매Benzyltrimethylammonium chlorideHCID 5963—
용매DichloromethaneHCID 6344—
생성물2-(Diphenylmethyleneamino)-3-(4-fluorophenyl)propanenitrileHCID 5845891092%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383639B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-bcd505dce2a9457487636a9990a7264e
출처 메모uspto-grants-2013_02