HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 1-methyl-1H-imidazole-2-carboximidamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Methyl-1H-imidazole-2-carbonitrile | HCID 10953443 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-methyl-1H-imidazole-2-carboximidamide hydrochloride | HCID 57415861 | 90.6% |
Reaction Steps
To 10 mL of methyl alcohol in a sealed tube is added sodium hydride (440 mg, 11 mmol) with stirring. 1-Methyl-2-imidazole carbonitrile (1.18 g, 11 mmol) is added. The mixture is stirred at room temperature for 20 h, and ammonium chloride (588 mg, 11 mmol) is added. The bottle is then sealed and stirred at 80° C. for 8 h, and cooled to room temperature. The mixture is filtered, and the filtrate is concentrated. The residue is treated with 1% methyl alcohol in diethyl ether, and the precipitates are collected by filtration and dried to give 1-methyl-2-imidazole carboxamidine hydrochloride as a gray solid (1.6 g). MS: m/z 125.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524849B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-7227f7d9235f4cfbb37c28f3ca1cff09 |
| Source note | uspto-grants-2009_04 |