HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-2-methyl-1-propene → 4-Methyl-7-methallyloxy-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 7-Hydroxy-4-methyl-1-indanone | HCID 12436244 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Methyl-7-methallyloxy-1-indanone | HCID 13604151 | — |
Reaction Steps
Into a solution of 15 g of 4-methyl-7-hydroxy-1-indanone and 7.95 g of potassium hydroxide in 200 ml of methanol was added 13.55 ml of methallyl chloride, and the mixture was refluxed by heating for 11 hours. The insoluble matters in the reaction mixture were removed by filtration, then 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 9 g of 4-methyl-7-methallyloxy-1-indanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04792628 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-cd8b7b060be64f7289e4470cda2668f0 |
| Source note | uspto-grants-1988_12 |