HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1,3-Cyclohexanedione, 2,5,5-trimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Dimedone | HCID 31358 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1,3-Cyclohexanedione, 2,5,5-trimethyl- | HCID 136901 | — |
Reaction Steps
28.0 g (0.2 mol) of dimedone were dissolved in 150 ml of absolute t-butanol and, at 40° C., 22.4 g (0.2 mol) of potassium t-butoxide were added a little at a time. After 2 hours, an equimolar amount of methyl iodide was added. After a further 2 hours, the solvent was removed under reduced pressure and the residue which remained was extracted 3 times with diethyl ether. The combined ether extracts were evaporated to dryness. Yield: 26.2 g (85%). The crude product was not purified further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06077965 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-32dc253c55404eaea20bbd9d01772a14 |
| Source note | uspto-grants-2000_06 |