HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → Imidazole, 1,2,4-trimethyl-5-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,4-Dimethyl-5-nitro-1H-imidazole (9CI) | HCID 135554430 | — |
| Solvent | Water | HCID 962 | — |
| Product | Imidazole, 1,2,4-trimethyl-5-nitro- | HCID 146466 | 58% |
Reaction Steps
2,4-dimethyl-5-nitroimidazole (7.0 g, 0.05 mole) and dimethylsulfate (7.0 ml, 0.074 mole) were heated at 100° C. for 1 hour 50 minutes. After cooling to room temperature, the reaction mixture was added to about 60 ml of water. Solid sodium bicarbonate was added until the solution is basic, and the mixture was then cooled on ice. The resulting crystals were filtered off and dried to give 6.2 g. This was recrystallized from water to give 4.5 g of 1,2,4-trimethyl-5-nitroimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04678799 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-cfa53942332b4d0795d58f53d70c3ebe |
| Source note | uspto-grants-1987_07 |