Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclohexyl phenyl ketone | HCID 12837 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Product | HCID 4115493 | HCID 4115493 | — |
Reaction Steps
To a suspension of methylbiphenylphosphonium iodide in dry THF cooled at 0° C. was added NaNH2. After stirring for 15 h at ambient temperature, cyclohexylphenyl ketone Was added. The reaction mixture was stirred for 8 h at ambient temperature and then quenched with aqueous ammonium chloride and extracted with ethyl acetate. The combined organic phases were washed (brine), dried (Na2SO4) and concentrated. Silica gel column chromatography of the crude product using petroleum ether:EtOAc (49:1) as eluent gave α-cyclohexylstyrene as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825378B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-25c94e98ef1d4caf83732f10246ce253 |
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| Source note | uspto-grants-2004_11 |
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