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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840449Generated: October 30, 2026

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

https://huagongshe.com/reaction/840449

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-ethylnyl-4,4-dimethyl-6-thiochromanmethanol were recovered in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06368608B1
Source datasetuspto-grants-2002_04
ORD IDord-97e57b796b224f49a02a7d79a8d0c1a8
Source noteuspto-grants-2002_04