HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 3-nitryloxy-2,2-bis(nitryloxymethyl)propionic acid N-benzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 2,2-bis(nitryloxymethyl)-3-nitryloxypropionate | HCID 15380869 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-nitryloxy-2,2-bis(nitryloxymethyl)propionic acid N-benzylamide | HCID 15380873 | 73% |
Reaction Steps
1 g (3.5 mmol) of methyl 3-nitryloxy-2,2-bis(nitryloxymethyl)propionate is heated with 3 ml of benzylamine and 100 ml of ammonium chloride for 3 hours at 130° C., cooled, taken up in 50 ml of chloroform and washed in sequence with water, dilute hydrochloric acid, aqueous bicarbonate solution and again with water. The crude product obtained after evaporating off the solvent is purified column chromatographically. 3-nitryloxy-2,2-bis(nitryloxymethyl)propionic acid N-benzylamide is obtained as a colourless oil. Yield: 73%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06365611B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-437a19c7e9c648319fc4ffaaba30cfb3 |
| Source note | uspto-grants-2002_04 |