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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802514Generated: November 3, 2026

1-Ethynylcyclohexanol → HCID 58399442, compound

https://huagongshe.com/reaction/1802514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-EthynylcyclohexanolHCID 6525—
Reactant4-MethylbenzaldehydeHCID 7725—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58399442HCID 5839944261%

Reaction Steps

To a solution of 1-ethynylcyclohexanol (500 mg, 4.02 mmol) in tetrahydrofuran (20 mL), 2.77 M n-butyllithium (solution in n-hexane, 3.6 mL, 9.90 mmol) was added dropwise at −78° C., and the obtained solution was stirred at the same temperature for 1 hour. To the reaction solution, p-tolualdehyde (0.52 mL, 4.40 mmol) was added at −78° C., and the obtained solution was allowed to warm gradually to room temperature with stirring. To the reaction solution, distilled water and 1 M hydrochloric acid were added to make the mixture acidic, and the resultant was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate) to obtain the captioned compound (598 mg, 2.44 mmol, 61%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349874B2
Source datasetuspto-grants-2013_01
ORD IDord-36002f4bce914a8f84c0c1a473a96560
Source noteuspto-grants-2013_01