HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218557Generated: October 31, 2026
Boron trifluoride etherate → 2-(o-Tolyl)cyclohexanol
https://huagongshe.com/reaction/2218557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Cyclohexene oxide | HCID 9246 | — |
| Reactant | 3-Bromotoluene | HCID 11560 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(o-Tolyl)cyclohexanol | HCID 251313 | — |
Reaction Steps
To a solution of 1-bromo-3-methyl-benzene in THF at −78° C., was added dropwise a solution of nBuLi (1.6M in THF, 12.4 ml) and the reaction mixture was stirred at −78° C. for 30 minutes. After such time, 7-oxa-bicyclo[4.1.0]heptane (3.4 g) was added slowly to the reaction mixture followed by the addition of boron trifluoride etherate (2.5 ml). The reaction mixture was stirred at −78° C. for another 2 hours before allowing it to warm up to room temperature. The solution was then treated with solution of ammonium chloride (25 ml), the phases were separated and then extracted twice with ethyl acetate. The combined organic extracts were then washed with water, dried over sodium sulfate and concentrated in vacuo. The residue was then purified by column chromatography to give 2.9 g of (cis/trans) 2-o-tolyl-cyclohexanol MS(EI) 190.1 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07411093B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-69dee6e1595449b08b1b5be0a4472616 |
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| Source note | uspto-grants-2008_08 |
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