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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1197241생성일: 2026년 10월 26일

N-Benzylideneaniline → N-(4-methylphenyl)-N-phenyl-benzenemethanamine

https://huagongshe.com/reaction/1197241

반응식

참여 물질

역할이름HCID투입량
반응물N-BenzylideneanilineHCID 10858—
반응물BenzyldiphenylamineHCID 69080—
반응물Benzyl p-tolyl etherHCID 70036—
생성물N-(4-methylphenyl)-N-phenyl-benzenemethanamineHCID 1570154551%

반응 단계

Methyl-4-(phenylmethoxy)benzene (1.98 g, 0.01 mol) and N-(phenylmethylene)benzenamine (1.81 g, 0.01 mol) were reacted in Na/DMF (1 g: 50 mL) at 75° C. for 30 min. Aqueous work-up, extraction with petroleum ether, 3×100 mL, and chromatography with petroleum ether/ethyl acetate 95:5 afforded a total of 1 g. of solid which by HPLC chromatography contained N,N-diphenyl-benzenemethanamine and the title compound in the ratio 6:94 (51% yield by HPLC). The purer fractions from chromatography on silica were combined and the solvent removed. The residual oil was dissolved in methanol and some petroleum ether. On cooling this crystallized the title compound. Two recrystallizations from methanol gave the title compound (98.1% pure; 36% yield), mp 85°-6° C. 1H NMR (200 MHz, CDCl3) δ(assignment): 2.29 (s, 3H, methyl), 4.97 (s, 2H, --NCH2Ph), 6.80-6.97 (m, 3H, aromatic) 7.06-7.27 (d, 4H, J=1.37 Hz, --NC6H4CH3), 7.14-7.36 (m, 7H, aromatic). MS [m/e (70 eV, % of base peak)]PhCH2N(Ph)(C6H4)CH3 272 (M+·, 96.5), 196 (M+· --Ph`, 31.7), 182 (M+· --PhCH3 ·, 100), 167 (M+· --PhCH2 ·--CH3·, 81.2), 91 (C7H7+, 98.3). FTIR (CDCL3): 3089, 3064, 3030, 2924, 2864, 1596, 1572, 1512, 1497, 1453 cm-1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05117062
출처 데이터셋uspto-grants-1992_05
ORD IDord-5dd01cc1f9be4e8a94d1680186b63a07
출처 메모uspto-grants-1992_05