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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347212Generated: October 25, 2026

Diethyl Ether → Cyclohexanol, 1-ethynyl-, 1-acetate

https://huagongshe.com/reaction/347212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1-EthynylcyclohexanolHCID 6525—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
CatalystScandium(III) triflateHCID 2734571—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductCyclohexanol, 1-ethynyl-, 1-acetateHCID 78903110.7%

Reaction Steps

To 3.1 g (25 mmol) 1-ethynyl-1-cyclohexanol in 25 ml acetonitrile were added 7.1 ml (75 mmol, 3 eq) acetic anhydride at −20° C. 12.3 mg (0.03 mmol) scandiumtriflate in 300 μl THF were added and the solution was stirred for 2 h. Additional 12.3 mg (0.03 mmol) scandiumtriflate in 300 μl THF were added and stirring was continued for 30 min. A saturated aqueous solution of NaHCO3 and ether were added. The layers were separated and the inorganic one was extracted with ether. The combined organic phases were washed with brine and dried over Na2SO4. Evaporation yielded 4.6 g crude 1-ethynylcyclohexyl acetate as colorless oil, MS: 166 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173043B2
Source datasetuspto-grants-2007_02
ORD IDord-ff95facf09e24a96b8ad7637b244ee47
Source noteuspto-grants-2007_02