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| | 5-Chloromethyl-1-methyl-1H-imidazole HCl Basic information |
| Product Name: | 5-Chloromethyl-1-methyl-1H-imidazole HCl | | Synonyms: | 4-(CHLOROMETHYL)-1-METHYL-1H-IMIDAZOLE;5-Chloromethyl-1-methyl-1H-imidazolehydrochloride;4-CHLOROMETHYL-1-METHYL-IMIDAZOLE HCL;4-chloromethyl-1-methyl-imidazole Hydrochloride;4-(ChloroMethyl)-1-Methyl-1H-iMidazole hydrochloride;5-Chloromethyl-1-methyl-1H-imidazole HCl | | CAS: | 17289-30-4 | | MF: | C5H7ClN2 | | MW: | 130.57548 | | EINECS: | | | Product Categories: | | | Mol File: | 17289-30-4.mol |  |
| | 5-Chloromethyl-1-methyl-1H-imidazole HCl Chemical Properties |
| Melting point | 153-154 °C | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | Appearance | White to off-white Solid |
| | 5-Chloromethyl-1-methyl-1H-imidazole HCl Usage And Synthesis |
| Synthesis | At 0 °C, (1-methyl-1H-imidazol-4-yl)methanol (5 g, 44.64 mmol) was dissolved in dichloromethane (10 mL) and thionyl chloride (50 mL) was added slowly and dropwise. The reaction mixture was stirred overnight at room temperature and then refluxed for 3 hours. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure. The residue was treated with diethyl ether and the resulting precipitate was filtered and dried to give 4-(chloromethyl)-1-methyl-1H-imidazole hydrochloride as a brown solid (4 g, 53.80% yield). The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 9.25 (s, 1H), 7.8 (s, 1H), 4.95 (s, 2H), 3.9 (s, 3H). | | References | [1] Patent: WO2004/13134, 2004, A2. Location in patent: Page 26
[2] Patent: WO2004/13135, 2004, A1. Location in patent: Page 47
[3] Patent: WO2004/13138, 2004, A2. Location in patent: Page 23 |
| | 5-Chloromethyl-1-methyl-1H-imidazole HCl Preparation Products And Raw materials |
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