HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Bromo-1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 5-Bromo-1,3-dihydro-2H-benzimidazol-2-one | HCID 12228060 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | 5-Bromo-1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-one | HCID 47003447 | — |
Reaction Steps
Iodomethane (2.41 g) was added to a suspension of 5-bromo-1,3-dihydro-benzoimidazol-2-one (1.65 g) and potassium tert-butoxide (1.91 g) in DMA (20 ml). The mixture was stirred overnight at room temperature. The mixture was poured to 2.5N aqueous HCl (80 ml) and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and then concentrated in vacuo. Heptane (50 ml) was added to the residue and the mixture was filtered. The residue was washed with diethyl ether and dried in vacuo to give the title compound (1.1 g) as a light brown solid. MS (m/e)=241.1 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268820B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-fee2e925739c48ef8a0c41283ff96c9f |
| Source note | uspto-grants-2012_09 |