HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635573Generated: October 31, 2026
Diethyl Ether → 1-[(2-Chlorophenyl)methyl]-4,5-dimethyl-1H-imidazole
https://huagongshe.com/reaction/1635573
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | alpha-Bromo-o-chlorotoluene | HCID 11905 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 18676173 | HCID 18676173 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[(2-Chlorophenyl)methyl]-4,5-dimethyl-1H-imidazole | HCID 12011183 | 44.8% |
Reaction Steps
To a solution of 4.89 g (0.027 mol) of 4,5-dimethylimidazole hydrobromide and 5.7 g (0.028 mol) of 2-chlorobenzyl bromide in 20 ml of DMF is added 6 ml of 50% potassium hydroxide aqueous solution dropwise. Then the reaction mixture is stirred at RT under nitrogen overnight. The reaction mixture is poured into ether (100 ml)/ water (50 ml). The ether layer is separated, washed with water (10 ml×2), dried over anhydrous sodium sulfate and evaporated in vacuo. The raw material is subjected to chromatography on silica gel using dichloromethane-methanol (10:1) as eluent to give 2.67 g (44%) of 1-(2′-chlorobenzyl)-4,5-dimethylimidazole as a pale yellow oil. MS m/z (M++1) 221; 1H-NMR 400 MHz(δ, CDCl3): 2.00 (3H, s), 2.20 (3H, s), 5.07 (2H, s), 6.59 (1H, dd, J=9.2, 2 Hz), 7.17 (1H, td, J=8, 1.2 Hz), 7.23 (1H, td, J=8, 1.6 Hz), 7.38 (2H, dd, J=7.2, 1.6 Hz) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06509366B2 |
|---|
| Source dataset | uspto-grants-2003_01 |
|---|
| ORD ID | ord-5131e08a8d4a47529f9e5e47e8cf73aa |
|---|
| Source note | uspto-grants-2003_01 |
|---|