Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11084070 | HCID 11084070 | — |
Reaction Steps
Ex-18a) A suspension of potassium t-butoxide in toluene cooled to 0° C. in an ice bath under N2 is treated with cyclohexanone. To the reaction mixture is slowly added 3-butenyl bromide. The reaction is warmed to room temperature. The reaction is then poured into EtOAc and washed once with 10% potassium hydrogen sulfate. The organic solution is then washed with brine, dried over magnesium sulfate, and the solvent evaporated under reduced pressure to afford 2-(3-butenyl) cyclohexanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06774126B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-2821b8840ce348a6ad0203d5f827e5da |
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| Source note | uspto-grants-2004_08 |
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