HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 21538594, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4,6-Dimethylpyridin-2-ol | HCID 226288 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21538594 | HCID 21538594 | — |
Reaction Steps
A mixture of 4,6-dimethyl2(1H)-pyridone (2.46 g., 0.02 moles), potassium hydroxide (1.58 g., 0.024 moles) and ethyl iodide (6.24 g., 0.04 moles) in 50 ml. ethanol is heated at reflux for 3 hours. The ethanol is removed under vacuum leaving a solid residue which is extracted with methylene chloride. The methylene chloride extracts are washed with 2.5 N sodium hydroxide, water, a saturated salt solution, and dried over sodium sulfate. Evaporation of the dried extracts affords 1-ethyl-4,6-dimethyl-2(1H)-pyridone as a pale yellow oil (1.5 g., 48%) which shows a single spot on thin layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03957997 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-0112d6e67f9b4b5baf238050d3548d48 |
| Source note | uspto-grants-1976_05 |