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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262875Generated: November 1, 2026

Acetic Acid → 3-TETRAHYDROPYRANYLOXY-1-TRIMETHYLSILYL-1-PROPYNE

https://huagongshe.com/reaction/262875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product3-TETRAHYDROPYRANYLOXY-1-TRIMETHYLSILYL-1-PROPYNEHCID 1070378163.5%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a stirred -20° C. solution of 125 g. (0.89 mol.) of 3-tetrahydropyranyloxy-1-propyne (Example 56) in 450 ml of ether, under a nitrogen atmosphere, is added dropwise, over one hour, a solution of 45 ml (0.89 mol.) of 2.0 N n-butyllithium in hexane. After 150 ml of dry ether is added and the mixture stirred at -20° C. for 30 minutes, a solution of 98 g (0.89 mol.) of trimethylchlorosilane in 73 ml of ether is added dropwise. Stirring is continued for 30 minutes at -20° C and at ambient temperature for 18 hours. The reaction mixture is again cooled to -20° C., and a solution of 90 ml of acetic acid in 300 ml of ether is added dropwise, followed by 90 ml of water. It is then diluted with 500 ml of water, and extracted 3 times with 300 ml of 5% sodium bicarbonate solution. The organic phase is separated, washed with 500 ml of a saturated brine solution, dried over sodium sulfate, and eveporated at 40° C. under vacuum (12 mm.). The crude product is fractionally distilled, by 120°-125° C. (18 mm.), to yield 120 g of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154954
Source datasetuspto-grants-1979_05
ORD IDord-b63be3f2d0534a3eb2f7af27a0e510f0
Source noteuspto-grants-1979_05