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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042299Generated: November 1, 2026

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

https://huagongshe.com/reaction/2042299

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 numberUS08586546B2
Source datasetuspto-grants-2013_11
ORD IDord-079c1d24178e4c349a2ffcb5c0095285
Source noteuspto-grants-2013_11