HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4-(2,6-Dimethylphenyl)-2-pentanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(2,6-Dimethylphenyl)-3-buten-2-one | HCID 54292687 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2,6-Dimethylphenyl)-2-pentanone | HCID 21241886 | — |
Reaction Steps
To a mixture containing 20 g of CuI and 50 ml of tetrahydrofuran (THF) are added 105 ml of methyllithium dropwise during with agitation in a nitrogen atmosphere at a temperature of 0° C. or lower until the yellow precipitate barely dissolves. Then 8,7 g of 4-(2,6-dimethylphenyl)-3-buten-2-one in 50 ml of THF are added slowly at 0° C. The stirring is continued for an additional 2 h with a gradual increase of the temperature to +25° C. The reaction mixture obtained is hydrolysed with 300 ml of a solution of NH4Cl. The ether layer is removed, dried and evaporated to give the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04544664 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-35c9b02819ca4a8d8a069f4e7151b670 |
| Source note | uspto-grants-1985_10 |