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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1614433Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1614433

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-BenzylideneanilineHCID 10858—
EduktBenzyldiphenylamineHCID 69080—
EduktBenzyl p-tolyl etherHCID 70036—
LösungsmittelTolueneHCID 1140—
ProduktN-(4-methylphenyl)-N-phenyl-benzenemethanamineHCID 1570154551%

Reaktionsschritte

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 compund in the ratio 6:94 (51% yield by HPLC). The purer fractions from chromatograpy 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 compund (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 273 (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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05196606
Quelldatensatzuspto-grants-1993_03
ORD IDord-30f4ac1c70e842ae962c1b4236d3abbe
Quellennotizuspto-grants-1993_03