Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ozone | HCID 24823 | — |
| Reactant | HCID 12520963 | HCID 12520963 | — |
| Solvent | Oxygen | HCID 977 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19706767 | HCID 19706767 | — |
Reaction Steps
4,4-difluoro-3-ethyl-3-trimethylsilyloxy-5-hexene (2.00 g, 8.88 mmol) was dissolved in dichloromethane (80 ml), and the solution was cooled to -78° C. A gaseous mixture of O3 in O2 was passed into the solution until it became blue. Nitrogen was bubbled through the solution to remove excess ozone, dimethyl sulfide (3 ml) was added, and the solution was brought slowly to room temperature. Following ozonide decomposition, dichloromethane was added, and the organic layer was washed with water (twice), dried over CaCl2 and concentrated under reduced pressure. Flash chromatography (50 g silica gel; 5% EtOAc in petroleum ether as eluant) to give the title compound as a pale yellow oil, δ 0.14 (s 9H), 0.91 (m, 6H), 1.64 (m, 2H), 1.85 (m, 2H), 9.55 (t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05710142 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-8b8cee90fc9446d68f3921afdcdb9272 |
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| Source note | uspto-grants-1998_01 |
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