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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856540Generated: October 30, 2026

Chlorotrimethylsilane → 3-TETRAHYDROPYRANYLOXY-1-TRIMETHYLSILYL-1-PROPYNE

https://huagongshe.com/reaction/1856540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product3-TETRAHYDROPYRANYLOXY-1-TRIMETHYLSILYL-1-PROPYNEHCID 10703781—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a stirred -20° C. solution of 125 g. (0.89 mol.) of 3-tetraydropyranyloxy-1-propyne (Example 1) 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 a 5% sodium bicarbonate solution. The organic phase is separated, washed with 500 ml. of a saturated brine solution, dried over sodium sulfate, and evaporated at 40° C. under vacuum (12 mm.). The crude product is fractionally distilled, b.p. 120°-125° C. (18 mm.), to yield 120 g. of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04219664
Source datasetuspto-grants-1980_08
ORD IDord-bf9616a659f84efcb2a6debfaae36c9a
Source noteuspto-grants-1980_08