HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342353Generated: October 30, 2026
Water → 4-(2-(4-n-Propylphenyl)ethenyl)cyclohexanone
https://huagongshe.com/reaction/342353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Oxocyclohexane-1-carbaldehyde | HCID 11170973 | — |
| Reactant | 4-n-Propylbenzyltriphenyl phosphonium bromide | HCID 23118839 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-(4-n-Propylphenyl)ethenyl)cyclohexanone | HCID 53917570 | 72.3% |
Reaction Steps
Suspension of 114 g of 4-n-propylbenzyltriphenyl phosphonium bromide in 500 ml of THF was stirred under nitrogen gas stream and 32.3 g of potassium-t-butoxide was added thereto at room temperature. After stirred at room temperature for 1 hour, a solution of 31.2 g of 4-formylcyclohexanone in 200 ml of THF was added dropwise to the suspension. After stirred at room temperature for 2 hours, 1 l of water was added thereto and then it was extracted with 1 l of ethyl acetate. Organic layer was washed with water and dried over anhydrous magnesium sulfate, the solvent was distilled off under a reduced pressure, and then 500 ml of heptane was added thereto. Precipitate thus separated was filtered off and purified by a column chromatography over a silica gel by using ethyl acetate/heptane (1/5) as an eluent, and the solvent was distilled off under a reduced pressure to obtain 42 g of 4-(2-(4-n-propylphenyl)ethenyl)cyclohexanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05858275 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-33b5b69282e94b6a9042cc103cecc836 |
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| Source note | uspto-grants-1999_01 |
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