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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840448Generated: October 31, 2026

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

https://huagongshe.com/reaction/840448

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 numberUS06368608B1
Source datasetuspto-grants-2002_04
ORD IDord-22ca85786dc54007b7021d2f324c09eb
Source noteuspto-grants-2002_04