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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252200Generated: October 30, 2026

Benzyl Chloride → 2-Amino-1-benzylbenzimidazole

https://huagongshe.com/reaction/252200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
Reactant2-AminobenzimidazoleHCID 13624—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product2-Amino-1-benzylbenzimidazoleHCID 17074239%

Reaction Steps

To a solution of 2-aminobenzimidazole (2) (Aldrich, 6 g., 45 mmol) in EtOH (10 mL) was added EtONa (21% in EtOH, 16.83 mL, 45 mmol) and benzyl chloride (5.70 mL, 50 mmol) and the brown solution was refluxed for 3 days under N2 gas. After cooling to room temperature, the reaction mixture was filtered through celite and concentrated in vacuo. The resulting brown solid was filtered hot in 300 mL acetone and crystallized from approximately 100 mL of acetone, and gave 3 as brown crystals (3.91 g., 39%). Recrystallization of the mother liquor afforded additional 3 as brown crystals (0.70 g., 7%). 1H-NMR (DMSO-d6) δ 5.27 (s, 2H), 6.61 (s, 2H), 6.82 (t, J=8.8 Hz, 1H), 6.93 (t, J=6.4 Hz, 1H), 7.05 (d, J=8.0 Hz, 1H), 7.15 (d, 7.2 Hz, 1H), 7.20 (d, 6.8 Hz, 2H), 7.24 (d, 7.6 Hz, 1H), 7.31 (t, 7.6 Hz, 2H); 13C-NMR (DMSO-d6) 45.11, 108.30, 115.19, 118.49, 120.88, 127.39, 127.66, 128.91, 134.60, 137.64, 143.34, 155.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868028B2
Source datasetuspto-grants-2011_01
ORD IDord-a1bb42c2b1844d15a110df80e4d73138
Source noteuspto-grants-2011_01