HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-Methyl-7-allyloxy-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 7-Hydroxy-4-methyl-1-indanone | HCID 12436244 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Methyl-7-allyloxy-1-indanone | HCID 13604147 | — |
Reaction Steps
Into a solution of 36 g of 4-methyl-7-hydroxy-1-indanone and 17.6 g of potassium hydroxide in 650 ml of methanol was added 25 ml of allyl bromide, and the mixture was refluxed by heating for 6 hours. The insoluble matters in the reaction mixture were removed by filtration, then the solvent was removed by evaporation. The residue obtained was extracted with chloroform-water, and the chloroform layer was collected by separation, then the solvent was removed by evaporation. The residue thus obtained was washed with ether and purified by means of a column chromatography to obtain 32 g of 4-methyl-7-allyloxy-1-indanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04792628 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-2371e098b30d4753b8b9758abde13125 |
| Source note | uspto-grants-1988_12 |