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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantCyclohexene oxideHCID 9246—
Reactant3-BromotolueneHCID 11560—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(o-Tolyl)cyclohexanolHCID 251313—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07411093B2
Source datasetuspto-grants-2008_08
ORD IDord-69dee6e1595449b08b1b5be0a4472616
Source noteuspto-grants-2008_08