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 % 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. Recrytallization 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 | US03951989 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-6eb5b8aff02140328c45c5a375156924 |
| Source note | uspto-grants-1976_04 |