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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Tetrahydro-2-(2-propynyloxy)-2H-pyran | HCID 98609 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-TETRAHYDROPYRANYLOXY-1-TRIMETHYLSILYL-1-PROPYNE | HCID 10703781 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04219664 |
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| Source dataset | uspto-grants-1980_08 |
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| ORD ID | ord-bf9616a659f84efcb2a6debfaae36c9a |
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| Source note | uspto-grants-1980_08 |
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