HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 6-chloropyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178498304 | HCID 178498304 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 6-chloropyridine-3-carboxylate | HCID 254249 | — |
Reaction Steps
In 100 ml of acetonitrile was dissolved 4.0 g (0.026 mole) of methyl 6-hydroxynicotinate followed by addition of 0.9 ml of triethylamine. The mixture was refluxed and 3.7 ml of phosphorus oxychloride was added dropwise with stirring over a period of 15 minutes. The mixture was further refluxed for 3 hours. After cooling, the acetonitrile was distilled off and the residue was diluted with 20 ml of water and adjusted to pH about 8 with a saturated aqueous solution of sodium hydrogen carbonate. The resulting crystals are collected by filtration, rinsed with water and dried to give 3.6 g of methyl 6-chloronicotinate as pale yellow needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05214152 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-ea6f6b006e9e46feb67ccdcfb0120f4b |
| Source note | uspto-grants-1993_05 |