HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-aminopyridine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Acetamidopyridine-4-carboxylic acid | HCID 3774466 | — |
| Product | Ethyl 2-aminopyridine-4-carboxylate | HCID 7015521 | 79% |
Reaction Steps
2-Acetylamino-isonicotinic acid (10.8 g, 60.0 mmol) was suspended in ethanol (150 mL) and BF3OEt2 (22 mL, 138 mmol) was added. The mixture was refluxed overnight, and after cooling to room temperature 10% NaHCO3 (250 mL) was added. The product was extracted with chloroform and the combined organic extracts were washed with water and dried. Filtering and concentration afforded 2-amino-isonicotinic acid ethyl ester (7.46 g, 79%) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071175B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-cecb5bf832084ef5a6421240cee3dddf |
| Source note | uspto-grants-2006_07 |