HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → Ethyl 2,6-bis(trifluoromethyl)-4-ethoxy-5-methyl-3-pyridinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178469144 | HCID 178469144 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2,6-bis(trifluoromethyl)-4-ethoxy-5-methyl-3-pyridinecarboxylate | HCID 13882898 | 77.7% |
Reaction Steps
A mixture of 7.8 g (0.0246 mol) of product of Example 35, 3.5 g of K2CO3, 20 g of iodoethane, and 100 ml of acetone was held at reflux for 2 days and concentrated. The reaction mixture was treated with 150 ml of water and extracted with 200 ml of ether. The ether extract was dried and concentrated. The residual solid (7.5 g) was recrystallized from hexane at low temperature to give 6.6 g (77.7%) of product; mp 72.5°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04655816 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-ed90bfa9b6184f019218d6eacc6e66a4 |
| Source note | uspto-grants-1987_04 |