Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278720Generated: November 2, 2026

O-Phenylenediamine → (E)-2-[2-(3,4-Dimethoxyphenyl)-vinyl]-1H-benzoimidazole

https://huagongshe.com/reaction/1278720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantHydrate;hydrochlorideHCID 21885828—
ReactantMethyl-(3,4-dimethoxy)-cinnamoimidate hydrochlorideHCID 86758495—
SolventMethanolHCID 887—
Product(E)-2-[2-(3,4-Dimethoxyphenyl)-vinyl]-1H-benzoimidazoleHCID 583465080%

Reaction Steps

A mixture of 1,2-phenylenediamine (0.63 g; 5.8 mmol) and methyl-(3,4-dimethoxy)-cinnamoimidate hydrochloride (1.5 g; 5.8 mmol) in methanol (35 mL) was stirred at ambient temperature for 18 hours. The methanol solution was concentrated to dryness. The residue was recrystallized from MeOH-Diethyl Ether to obtain 1.3 g (67% yield) of the title compound as a mono-hydrochloride, hydrate, yellow solid, m.p. 248° C. dec. Anal. Calcd. for C17H16N2O2 HCl H2O: C, 60.98, H, 5.12; N, 8.37. Found: C, 60.78; H, 5.12; N, 8.45. Mass Spectrum: (EI; M+) m/z 280..1H-NMR (DMSO-d6; 400 MHz) δ15.2 (broad s, 1H), 8.18-8.2 (d, 1H), 7.76-7.8 (m, 2H), 7.45-7.54 (m, 2H), 7.32 (d 1H), 7.2-7.3 (m, 3H), 7.08-7.12 (d, 1H), 3.83 (s, 3H), 3.86 ppm (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444694B1
Source datasetuspto-grants-2002_09
ORD IDord-cb43e4461c64430ea50f9194c7340d9a
Source noteuspto-grants-2002_09