Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 2-Chloro-4-methyl-3-nitropyridine | HCID 345363 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86619018 | HCID 86619018 | 81.6% |
Reaction Steps
To a heterogeneous solution of potassium ethoxide (6.56 g, 77.9 mmol) in diethyl ether (55 mL), was slowly added diethyl oxalate (10.6 mL, 77.9 mmol). A slight exotherm resulted. After stirring 5 min, a homogeneous yellow solution resulted, but after 10 min, a heterogeneous yellow slurry was observed. Addition of 2-chloro-4-methyl-3-nitropyridine (13.45 g, 77.9 mmol) as a solid, with a diethyl ether rinse (23 mL), resulted in a dark violet solution with a dark precipitate. The mixture was stirred at room temperature overnight (21 h). The solid precipitate was filtered, rinsed thoroughly with diethyl ether, and air-dried to give potassium (1Z)-1-(2-chloro-3-nitropyridin-4-yl)-3-ethoxy-3-oxoprop-1-en-2-olate (19.8 g, 63.6 mmol, yield 81%) as an orange solid. The crude product was used directly without further purification or identification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07608627B2 |
|---|
| Source dataset | uspto-grants-2009_10 |
|---|
| ORD ID | ord-b9ac46418dce47f389fdb4613caa8cdd |
|---|
| Source note | uspto-grants-2009_10 |
|---|