HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Methyl 2-(3-nitropyridin-2-yloxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl Glycolate | HCID 66774 | — |
| Reactant | 2-Chloro-3-nitropyridine | HCID 79613 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 2-(3-nitropyridin-2-yloxy)acetate | HCID 12115511 | 70.5% |
Reaction Steps
0.4 g of sodium hydride was added to a mixture of 1.59 g of 2-chloro-3-nitropyridine, 0.95 g of methyl glycolate and 10 ml of 1,4-dioxane at 10° C. The mixture was stirred at room temperature for 2 hours, then, the reaction solution was poured into ice water, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 1.5 g of 2-(methoxycarbonyl)methoxy-3-nitropyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06537948B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-928703258bed4997b0ef2dcab2c5d316 |
| Source note | uspto-grants-2003_03 |