HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 12428607, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178469712 | HCID 178469712 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12428607 | HCID 12428607 | — |
Reaction Steps
A mixture of 1.38 parts of ethyl 4-hydroxy-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridine-3-carboxylate, 11 parts by volume of 10 percent aqueous potassium hydroxide, 44 parts by volume of ethanol and 45 parts by volume of water and 1.5 parts by volume of ethyl iodide is refluxed for 4 hours and the product is isolated in a manner similar to that described in Example 13, whereby 1-ethyl-1,4,5,6,7,8-hexahydro-4-oxo[1]benzothieno[2,3-b]pyridine-3-carboxylic acid is obtained as crystals. Recrystallization from ethanol and, then, from tetrahydrofuran gives colorless needles melting at 218°-221° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997545 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-60a4c8b767c547efa676ef969e9731c8 |
| Source note | uspto-grants-1976_12 |