HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → Ethyl 5-methyl-3-nitromethylheptanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Ethyl 5-methyl-2-heptenoate | HCID 53937332 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 5-methyl-3-nitromethylheptanoate | HCID 21888385 | 42% |
Reaction Steps
Ethyl 5-methyl-2-heptanoate 12 (6.75 g, 39.70 mmol), DBU (6.0 g, 39.7 mmol), nitromethane (21.97 g, 359.9 mmol) in acetonitrile 80 mL was stirred at room temperature under nitrogen atmosphere overnight. The mixture was concentrated to an oil. A solution of the oil in ether was washed with 1N HCl, brine and dried. It was evaporated to give a light oil which was chromatographed on silica gel, eluting with 5% to 10% ether in Pet. ether to give 13 (3.6 g, 42%). 1H-NMR (CDCl3) δ4.49-4.39 (m), 4.12-4.07 (m), 3.61 (m), 2.36 (m), 1.36-1.18 (m), 0.86-0.79.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06642398B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-3bd189e0a2004685ab53c3678dd2e926 |
| Source note | uspto-grants-2003_11 |