HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → 3-(2-Nitro-2-methylpropyl)-7-nitroindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Indole, 3-((dimethylamino)methyl)-7-nitro- | HCID 15451 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | 2-Nitropropane | HCID 398 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(2-Nitro-2-methylpropyl)-7-nitroindole | HCID 22014767 | 131% |
Reaction Steps
The 7-nitrogramine salt (2.0 g, 5.8 mmol) is suspended in a mixture of 2-nitropropane (9.5 mL) and methanol (9.5 mL). Dimethylsulfate (1.09 mL, 11.5 mmol) is added dropwise via syringe, and the resulting yellow solution is stirred at room temperature for 5 minutes. Sodium methoxide (0.62 g, 11.5 mmol) is then added in one portion, and the mixture is stirred overnight at room temperature. The reaction is quenched by addition of saturated NH4Cl solution and ethyl acetate. The aqueous layer is extracted with ethyl acetate, and the combined organic layers are washed with brine, and dried over Na2SO4 to give 1.0 g of 3-(2-nitro-2-methylpropyl)-7-nitroindole (69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06911463B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-5ba55724ebce42ff82d349d65ee36bd6 |
| Source note | uspto-grants-2005_06 |