HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252200Generated: October 30, 2026
Benzyl Chloride → 2-Amino-1-benzylbenzimidazole
https://huagongshe.com/reaction/252200
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 2-Aminobenzimidazole | HCID 13624 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-1-benzylbenzimidazole | HCID 170742 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868028B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-a1bb42c2b1844d15a110df80e4d73138 |
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| Source note | uspto-grants-2011_01 |
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