HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → 2,6-Bis(trifluoromethyl)-3-methoxycarbonyl-4-chloropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Methyl 2,6-bis(trifluoromethyl)-4-hydroxy-3-pyridinecarboxylate | HCID 178498966 | — |
| Product | 2,6-Bis(trifluoromethyl)-3-methoxycarbonyl-4-chloropyridine | HCID 13882878 | 19.7% |
Reaction Steps
A mixture of 6.7 g (0.0232 mol) of product of Example 4, 2.8 g (0.026 mol) of 2,6-lutidine, and 50 ml of POCl3 was held at reflux for 18 hours and concentrated. The residue was treated with water and extracted with ether. The ether extract was washed with 10% NaOH and then with saturated NaCl, dried, and concentrated. The residue was kugelrohr distilled at 133 Pa (pot temperature 90° C.). The distillate was recrystallized from hexane at low temperature to give 1.4 g (19.7%) of product; mp 48°-49° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04655816 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-e3e49325bc584731ad8b270fd87a4e03 |
| Source note | uspto-grants-1987_04 |