HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132104Generated: October 25, 2026
Cyclohexanone → 1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanol
https://huagongshe.com/reaction/132104
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | 1-Bromo-3-tert-butylbenzene | HCID 343798 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanol | HCID 59733743 | 81% |
Reaction Steps
A solution of 1.7 M tert-butyllithium in pentane (32.0 mL, 54.4 mmol) was added to a solution of 1-bromo-3-tert-butyl-benzene (5.54 g, 26.0 mmol) in tetrahydrofuran (60 mL) at −78° C. After stirring for 1 h, cyclohexanone (2.00 g, 18.2 mmol) in tetrahydrofuran (15 mL) was added. After stirring for 18 h, during which time the solution warmed to ambient temperature, the solution was diluted with saturated aqueous ammonium chloride and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was flash chromatographed with 49:1, 24:1, 23:2 hexanes:ethyl acetate as the eluant to yield 3.61 g (81% yield) of 1-(3-tert-butyl-phenyl)-4-methylene-cyclohexanol as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07385085B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-f0668dfcdcd04782a255a587cf61429e |
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| Source note | uspto-grants-2008_06 |
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