HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (E)-N-methyl-N'-nitromethoxymethanimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | O-methyl-N-nitroisourea | HCID 136196430 | — |
| Solvent | Water | HCID 962 | — |
| Product | (E)-N-methyl-N'-nitromethoxymethanimidamide | HCID 136414659 | 73% |
Reaction Steps
Into a 100-ml, 4-necked flask equipped with a stirrer were introduced 1.5 g of O-methyl-N-nitroisourea, 11 g of water, 3 g of sodium chloride and 2 g of methylamine hydrochloride, and the resulting material was maintained at 20 degree centigrade. Thereafter, 0.1 g of sodium hydrogen carbonate was added to the mixture and the mixture was stirred at 20 degree centigrade for 16 hours. Then, while stirring the reaction mixture, 0.1 g of concentrated hydrochloric acid and 200 ml of water were added to the mixture to give a homogenious aqueous solution of N,O-dimethyl-N′-nitroisourea, which was analyzed by HPLC. In the aqueous solution, 1.2 g of N,O-dimethyl-N′-nitroisourea was contained, and the reaction yield was 73%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560593B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-15b83ee7c312454993f215a4be1df0f0 |
| Source note | uspto-grants-2009_07 |