HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 2825021, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 7-Hydroxy-2,2,5-trimethyl-2,3-dihydro-4H-1-benzopyran-4-one | HCID 2727964 | — |
| Solvent | Potassium | HCID 5462222 | — |
| Product | HCID 2825021 | HCID 2825021 | 85% |
Reaction Steps
In 50 ml of acetonitrile 4.9 g (20 millimoles) of the potassium salt of 7-hydroxy-2,2,5-trimethyl-4-chromanone are dissolved and the solution is stirred in the presence of 0.5 g (2 millimoles) of 18-Crown-6 at room temperature for 30 minutes. To the mixture 4.25 g (1.9 ml, 30 millimoles) of methyl iodide are added and the reaction mixture is stirred for a further hour. The inorganic salt is filtered off and the solvent is removed. The residue is taken up in chloroform, washed twice with 50 ml of water each, dried over sodium sulfate and evaporated. The product is crystallized from 90% ethanol. Thus 3.75 g of the desired compound are obtained, yield 85%. Mp.: 86°-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04866089 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-d1b2ae970e3647928d1873f68bec5d4d |
| Source note | uspto-grants-1989_09 |