HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 70605160, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178526372 | HCID 178526372 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70605160 | HCID 70605160 | — |
Reaction Steps
Potassium t-butoxide, 3.15 g (0.0281 moles) was added to a mixture of 70 ml of dimethylformamide and 14 ml of nitromethane. After stirring for 30 min at room temperature under nitrogen, 6.9 g (0.0234 moles) of 3,5-dihydro-2-(N-nitrosomethylamino)-5-phenyl-4H-1,5-benzodiazepin-4-one, was added and stirring was continued for 48 hours. The mixture was acidified with acetic acid and diluted with water. The precipitate was collected, washed with water and recrystallized from methylene chloride/ethanol to yield end product with mp 231°-234°. Recrystallization for analysis from the some solvents raised the melting point to 233°-235°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04146537 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-e5d67f3b000c4261b61b4587902ee82b |
| Source note | uspto-grants-1979_03 |