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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466808Generated: October 29, 2026

Cyclohexanol, 1-((trimethylsilyl)ethynyl)- → 1-Ethynylcyclohexanol

https://huagongshe.com/reaction/466808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanol, 1-((trimethylsilyl)ethynyl)-HCID 205445—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
Product1-EthynylcyclohexanolHCID 6525—

Reaction Steps

Dissolve 1-(2-trimethylsilyl-1-ethynyl)cyclohexanol (1.79 g, 9.13 mmol) in tetrahydrofuran (11 mL) and place under an argon atmosphere. Add, by dropwise addition, tetra-n-butylammonium fluoride (11 mL of a 1M solution in tetrahydrofuran, 11 mmol). Stir for 1 hour at room temperature and partition between methylene chloride and water. Separate the organic phase, wash with saturated aqueous sodium chloride, dry (MgSO4), filter and evaporate the solvent in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157167
Source datasetuspto-grants-1992_10
ORD IDord-9407aa3917b1401fb09b205273d463da
Source noteuspto-grants-1992_10