HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-Methyl-7-crotyloxy-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Butene, 1-bromo- | HCID 122414 | — |
| Reactant | 7-Hydroxy-4-methyl-1-indanone | HCID 12436244 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Methyl-7-crotyloxy-1-indanone | HCID 53634370 | — |
Reaction Steps
Into a solution of 10 g of 4-methyl-7-hydroxy-1-indanone and 5.3 g of potassium hydroxide in 200 ml of methanol was added 8.2 ml of crotyl bromide, and the mixture was refluxed by heating for 4 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 washed with a diluted sodium hydroxide aqueous solution, then washed with water, dried with anhydrous magnesium sulfate, and the solvent was removed by evaporation. The residue obtained was purified by means of a silica gel column chromatography (eluent: n-hexane: dichloromethane=1:1) to obtain 8.72 g of 4-methyl-7-crotyloxy-1-indanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04792628 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-c5e1de5bb72f45a59afd3faaff265cc2 |
| Source note | uspto-grants-1988_12 |