HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227841Generated: October 26, 2026
Hydrochloric Acid → (E)-N-methyl-N'-nitromethoxymethanimidamide
https://huagongshe.com/reaction/227841
Participants
| Role | Name | HCID | Charge |
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| 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 | 717.9% |
Reaction Steps
Into a 2000-ml, 4-necked flask equipped with a stirrer were introduced 121 g of O-methyl-N-nitroisourea, 907 g of water, 250 g of sodium chloride and 172 g of methylamine hydrochloride, and the resulting material was maintained at 20 degree centigrade. Thereafter, 8 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, 3.5 g of concentrated hydrochloric acid was added to the mixture. After, the reaction mixture was cooled with ice, the precipitated N,O-dimethyl-N′-nitroisourea was collected by filteration, washed with cold water, and then dried. 91 g of an N,O-dimethyl-N′-nitroisourea crystal with a purity of 99% was obtained. The isolated yield was 67%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560593B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-b724543548c942fbac4075432894d035 |
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| Source note | uspto-grants-2009_07 |
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