HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622704Generated: October 25, 2026
Dimethylformamide → 1-(3-Methoxy-2-nitro-6-methylpyridylmethyl)-2-nitromethyleneimidazolidine
https://huagongshe.com/reaction/622704
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Nitromethylene)imidazolidine | HCID 3014763 | — |
| Reactant | 3-Methoxy-2-nitro-6-pyridylmethyl bromide | HCID 14405124 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | 1-(3-Methoxy-2-nitro-6-methylpyridylmethyl)-2-nitromethyleneimidazolidine | HCID 86742440 | — |
Reaction Steps
Nitromethyleneimidazolidine (1.3 g) was dissolved in dry dimethylformamide (15 ml), and sodium hydride (0.26 g) was added. The mixture was stirred at room temperature until the generation of hydrogen ceased. Subsequently, a solution of 2.4 g of 3-methoxy-2-nitro-6-pyridylmethyl bromide in 5 ml of dimethylformamide was added, and the mixture was stirred at 60° C. for 15 minutes. The reaction mixture was cooled to room temperature, poured into 50 ml of ice water, and extracted with dichloromethane. Dichloromethane was distilled off under reduced pressure, and ethanol was added to the residue to precipitate crystals. The crystals were collected by filtration and washed with ethanol to give 1-(3-methoxy-2-nitro-6-methylpyridylmethyl)-2-nitromethyleneimidazolidine (0.4 g). mp. 177°-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04772620 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-4cdc866464844c1c9043c9b082818713 |
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| Source note | uspto-grants-1988_09 |
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