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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861770Generated: November 1, 2026

Ammonium Chloride → alpha-Trimethylsilylethynyl-4,4-dimethyl-6-thiochromanmethanol

https://huagongshe.com/reaction/861770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant4,4-dimethyl-3,4-dihydro-2H-thiochromene-6-carbaldehydeHCID 15284308—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Productalpha-Trimethylsilylethynyl-4,4-dimethyl-6-thiochromanmethanolHCID 22361487100%

Reaction Steps

3 ml (21.3 mmol) of trimethylsilylacetylene and 50 ml of THF were introduced into a three-necked flask. A solution of 8.6 ml (21.3 mmol) of n-butyllithium (2.5M in hexane) was added dropwise at -78° C. under a stream of nitrogen and the reaction mixture was permitted to heat to room temperature. This solution was introduced dropwise into a solution of 4 g (19.4 mmol) of 4,4-dimethyl-6-thiochromancarboxaldehyde in 50 ml of THF at -78° C. The reaction mixture was permitted to heat to room temperature, was poured into an aqueous ammonium chloride solution and extracted with ethyl ether. The organic phase was separated by settling, dried over magnesium sulfate and evaporated. 5.9 g (100%) of the expected alcohol were obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716624
Source datasetuspto-grants-1998_02
ORD IDord-d10c1b695f624954bda323f1ee35a65f
Source noteuspto-grants-1998_02