Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 3,3,6-trimethyl-5-butoxy-indane | HCID 11333744 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 10171447 | HCID 10171447 | 75.5% |
Reaction Steps
100 g 3,3,6-trimethyl-5-butoxy-indane are dissolved in 400 g acetic acid and 1 g Co-II acetate is added. The reaction mixture is heated to 40° C., with stirring, and oxygen is passed through this solution for 10 hours. After cooling to room temperature, 500 g water and 500 g methyl tert.-butyl ether are added. After phase separation, the organic phase is rinsed with a further 200 g water and distilled in a 30 cm packed column. 80 g 3,3,6-trimethyl-5-butoxy-indan-1-one is obtained, which corresponds to a yield of 75% of theory. The compound can be recrystallised from heptane and a white solid is obtained, melting point: 59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235699B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-e95ca16bb51042ed9e3faaea669f8e17 |
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| Source note | uspto-grants-2007_06 |
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