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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640608Generated: October 30, 2026

Trimethyl orthobeznoate → 1-Benzyl-5-bromo-2-phenyl-1H-benzo[d]imidazole

https://huagongshe.com/reaction/1640608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthobeznoateHCID 69720—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-Benzylamino-5-bromoanilineHCID 28902906—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-5-bromo-2-phenyl-1H-benzo[d]imidazoleHCID 59133054—

Reaction Steps

p-TsOH.H2O (311.7 mg, 1.606 mmol) was added to a DCM (50 ml) solution of N1-benzyl-4-bromobenzene-1,2-diamine (4451 mg, 16.06 mmol) and trimethyl orthobenzoate (3096 μl, 17.66 mmol) and the resulting mixture was stirred at rt under an atmosphere of Nitrogen for 40 h. The reaction mixture was then concentrated in vacuo to give a yellow solid which was triturated with 40% MeOH/water (375 mL), filtered, washed with saturated NaHCO3 (20 ml)+H2O (80 ml) twice and 40% MeOH/H2O (2×50 ml), and dried to give the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm=5.44 (s, 2 H), 7.05-7.08 (m, 3 H), 7.30-7.36 (m, 4 H), 7.44-7.50 (m, 3 H), 7.66-7.68 (m, 2 H) and 7.99 (dd, 1 H, J=0.4 & 1.6 Hz). MS(ES+): m/z 363.20 and 365.26[MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114846B2
Source datasetuspto-grants-2012_02
ORD IDord-c1e8713479c64fd284fd296febc1a96a
Source noteuspto-grants-2012_02