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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086015Generated: October 25, 2026

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

https://huagongshe.com/reaction/1086015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BenzylideneanilineHCID 10858—
ReactantBenzyldiphenylamineHCID 69080—
ReactantBenzene, 1-chloro-4-(phenylmethoxy)-HCID 139062—
ProductN-(4-Chlorophenyl)-N-phenyl-benzenemethanamineHCID 12229151—

Reaction Steps

Chloro-4-(phenylmethoxy)benzene (2.18 g, 0.010 mol) and N-(phenylmethylene)benzenamine (1.81 g, 0.010 mol) were reacted in Na/DMF (1 g: 50 mL) at 50° C. for 7 hrs. The reaction was followed by HPLC to about 90% conversion. This technique indicated among other things the presence of the title compound, benzyldiphenylamine, and some unknown material in a ratio 65:18:17. Similar aqueous workup as for the preparation of benzyldiphenylamine and chromatography on silica gave 0.50 g of the title compound mp 94-5° C. from methanol (lit mp 97-7.5° C. 70% yield. This material is contaminated with a small amount of diphenylbenzylamine. 1H NMR (200 MHz, CDCl3)δ (assignment): 5.03 (s, 2H, Ph2NCH2Ph), 6.96-7.38 (m, 14H, aromatic). MS [m/e (70 eV, % of base peak)] C19H16ClN 293 (M+., 52.8), 295 (M+. +2, 28.8), 202 (M+. --C7H7+, 22), 167 (C6H4NPh)+., 48.3), 91 (C7H7+, 100). FTIR (CDCl3): 3066, 3033, 1589, 1494, 1454 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011998
Source datasetuspto-grants-1991_04
ORD IDord-8287c9582fbe465dbb688030f36dbb62
Source noteuspto-grants-1991_04