HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 3-Pyridinecarbonyl chloride, 6-(2,2,2-trifluoroethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 6-(2,2,2-Trifluoroethoxy)pyridine-3-carboxylic acid | HCID 2781028 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-Pyridinecarbonyl chloride, 6-(2,2,2-trifluoroethoxy)- | HCID 23512722 | 102% |
Reaction Steps
To 6-(2,2,2-trifluoro-ethoxy)-nicotinic acid (100 mg, 0.45 mmol) was added DCE (5 mL) and oxalyl chloride (60 ul, 0.68 mmol) under an atmosphere of nitrogen. The mixture was stirred at rt for 1.5 h then heated at 80 C for 2 h and after cooling to room temperature, evaporated to give the title compound as a pale yellow oil (110 mg, 100%). Method C HPLC-MS (in MeOH, identifying the methyl ester): MH+ requires m/z=236. Found: m/z=236, Rt=1.41 min (95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895733B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-d3be77bdd860451bb68698dc436494ad |
| Source note | uspto-grants-2014_11 |