HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1086014Erstellt: 24. Oktober 2026
N-Benzylideneaniline → N-(4-methylphenyl)-N-phenyl-benzenemethanamine
https://huagongshe.com/de/reaction/1086014
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-Benzylideneaniline | HCID 10858 | — |
| Edukt | Benzyldiphenylamine | HCID 69080 | — |
| Edukt | Benzyl p-tolyl ether | HCID 70036 | — |
| Produkt | N-(4-methylphenyl)-N-phenyl-benzenemethanamine | HCID 15701545 | 51% |
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 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, 4 H, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05011998 |
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| Quelldatensatz | uspto-grants-1991_04 |
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| ORD ID | ord-bb88a5714e9145898e13fa355669b723 |
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| Quellennotiz | uspto-grants-1991_04 |
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