Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 12806958 | HCID 12806958 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 20520799 | HCID 20520799 | — |
Reaction Steps
6,7-Dichloro-5-methoxy-2,3-dihydro-1H-inden-1-one (63.5 gm., 0.274 mole) is dissolved in a mixture of dry tert.-butyl alcohol (500 ml.) and dry benzene (1.5 liters). The solution is refluxed and potassium tert.-butoxide (46 gm., 0.301 mole) in dry tert.-butyl alcohol (1 liter) is added as rapidly as possible. The solution is refluxed for another 1/2 hour, cooled to 20° C., stirred and treated with allyl bromide (36 gm., 0.301 mole). The mixture is stirred and refluxed for 4 hours, cooled and treated with water (250 ml.). The crude 2-allyl-6,7-dichloro-5-methoxy-2,3-dihydro-1H-inden-1-one is separated by filtration, washed with water, dried and recrystallized from a mixture of benzene and hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04317922 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-63cbcf0b949f406893721069d54d0b25 |
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| Source note | uspto-grants-1982_03 |
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