HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-Methyl-1H-benzo[d]imidazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-Methyl-1H-benzo[d]imidazol-2-amine | HCID 676520 | 51.4% |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
2-Chloro-1H-benzo[d]imidazole (20 g, 131.08 mmol) was charged to high pressure autoclave PV10832 (Hastelloy 450 ml) with methylamine (260 mL, 131.08 mmol) and sealed on its trolley and the resulting solution heated to 160° C. in high pressure blast cell 60 for 16 hours. The pressure in the autoclave reached 11 bar. The solvent was removed under reduced pressure to afford a brown oil. EtOH was added and the solvent again removed to afford a brown foam. The foam was dissolved in a minimum of hot acetone. This was then allowed to cool. The resultant solid was filtered affording N-methyl-1H-benzo[d]imidazol-2-amine (9.91 g, 51%); 1H NMR (400 MHz, DMSO-d6) 2.83 (3H, s), 6.87-7.00 (2H, m), 7.05-7.25 (2H, m), 7.49 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552004B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-5c0be413ff594cd3bef580233e22be2c |
| Source note | uspto-grants-2013_10 |