HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Diiodopropane → 1,3-Bis[(6-chloronicotinyl)-2-nitroiminoimidazolidin-3-yl]propane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Diiodopropane | HCID 12314 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Imidacloprid | HCID 86287518 | — |
| Reactant | 1-[(6-chloropyridin-3-yl)methyl]-N-nitroimidazolidin-2-imine | HCID 135527764 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Bis[(6-chloronicotinyl)-2-nitroiminoimidazolidin-3-yl]propane | HCID 73706289 | — |
Reaction Steps
Sodium hydride (60% oil dispersion, 0.17 g, 4.25 mmol) was suspended in 10 ml of DMF. 1-(6-Chloronicotinyl)-2-nitroiminoimidazolidine (1.03 g, 4 mmol), which is commonly referred to as imidacloprid), was added to this suspension. This mixture was then stirred for 1 hour at room temperature. A solution of 1,3-diiodopropane (0.58 g, 2 mmol) in DMF (10 ml) was then added dropwise to this reaction mixture over the course of 30 minutes while cooling with ice. Following completion of dropping, the reaction mixture was stirred at room temperature for 4 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875778B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-df47b182e7cc4d1b8c2f82b58842e3bb |
| Source note | uspto-grants-2005_04 |