HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitroethane → 1-Hydroxy-2-methyl-3-oxidobenzimidazol-3-ium
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Benzofuroxan | HCID 68075 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Hydroxy-2-methyl-3-oxidobenzimidazol-3-ium | HCID 1476277 | 58.5% |
Reaction Steps
In the typical procedure, 0.1 mole of benzofurazan 1-oxide and 0.12 mole of nitroethane is dissolved at 100 ml. of tetrahydrofuran. To this mixture there is added at room temperature, 0.12 mole of diethylamine over a period of 0.5 hour. An instantaneous exothermic reaction is observed (40° C.) and within one hour, the product crystallizes from the solution. The solution is allowed to stand overnight at room temperature and filtered to yield 9.6 grams of 2-methyl-1-hydroxy-1-H-benzimidazole 3-oxide (Table III, Example H-77). The product can be recrystallized from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05001171 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-36347b557a35406f9617696326cf29be |
| Source note | uspto-grants-1991_03 |