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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086017Generated: October 25, 2026

Benzyldiphenylamine → 1-(Diphenylamino)-1-phenyl-2-(1-naphthyl)ethylene

https://huagongshe.com/reaction/1086017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyldiphenylamineHCID 69080—
Reactant(E)-1-(diphenylamino)-1-phenyl-2-phenylethyleneHCID 10948014—
SolventEthylacetate methanolHCID 21584119—
Product1-(Diphenylamino)-1-phenyl-2-(1-naphthyl)ethyleneHCID 53709022—

Reaction Steps

This compound was synthesized from diphenylbenzylamine and N-phenyl-1-naphthaldimine under the same conditions outlined for (E)-1-(diphenylamino)-1-phenyl-2-phenylethylene above. Recrystallizatiom from ethyl acetate/methanol gave small crystals mp 170-2° C. 1H NMR (200 MHz, CDCl3) δ (assignment): 6.60-6.90 (m, 2 H, aromatic), 6.80-7.38 (m, 15 H, aromatic), 7.52-7.85 (m, 6 H, aromatic). MS [m/e (70 eV, % of base peak] C10H7CHCPhNPh2 397 (M+., 43.1), 180 (PhCNPh+, 100), 77 (Ph+, 43.2); HRMS (m/z) for C30H23N (M+.), calcd. 397.183 found 397.195.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011998
Source datasetuspto-grants-1991_04
ORD IDord-70dc5fb1a1bc4b90ad8e2bae281cab6e
Source noteuspto-grants-1991_04