HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Lactate → 2-{1-(Methoxycarbonyl)ethoxy}-3-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Lactate | HCID 11040 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-3-nitropyridine | HCID 79613 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-{1-(Methoxycarbonyl)ethoxy}-3-nitropyridine | HCID 21933571 | 73% |
Reaction Steps
0.8 g of sodium hydride was added to a mixture of 3.17 g of 2-chloro-3-nitropyridine, 2.19 g of methyl lactate and 20 ml of 1,4-dioxane at 10° C. The mixture was stirred at room temperature for 1.5 hours, then, 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 3.3 g of 2-{1-(methoxycarbonyl)ethoxy}-3-nitropyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06537948B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-8c35a9af41644d81880d7f86246997aa |
| Source note | uspto-grants-2003_03 |