Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861771Generated: October 30, 2026

Tetrahydrofuran → alpha-Ethynyl-4,4-dimethyl-6-thiochromanmethanol

https://huagongshe.com/reaction/861771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactantalpha-Trimethylsilylethynyl-4,4-dimethyl-6-thiochromanmethanolHCID 22361487—
SolventWaterHCID 962—
Productalpha-Ethynyl-4,4-dimethyl-6-thiochromanmethanolHCID 22619414—

Reaction Steps

5.9 g (19.4 mmol) of α-trimethylsilylethynyl-4,4-dimethyl-6-thiochromanmethanol and 50 ml of THF were introduced into a round-bottomed flask and 21.3 ml (23.3 mmol) of a tetrabutylammonium fluoride solution (1.1M in THF) were added dropwise. Stirring was carried out at room temperature for 1 hour and the reaction mixture was poured into water and extracted with ethyl ether. The organic phase was separated by settling, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a silica column eluted with a mixture of ethyl acetate and hexane (1/4). After evaporating the solvents, 3.9 g (87%) of α-ethynyl-4,4-dimethyl-6-thiochromanmethanol were recovered in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716624
Source datasetuspto-grants-1998_02
ORD IDord-ffb69903eca14c55b97924e710bcf3bd
Source noteuspto-grants-1998_02