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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878879Generated: November 2, 2026

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

https://huagongshe.com/reaction/1878879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthobeznoateHCID 69720—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantN1-benzyl-5-bromobenzene-1,2-diamineHCID 65343042—
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 N′-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 numberUS08314111B2
Source datasetuspto-grants-2012_11
ORD IDord-efed9110a125474c9bdbe8e6d8606200
Source noteuspto-grants-2012_11