HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582516Generated: November 2, 2026
Silane, chlorodimethyl(3,3,3-trifluoropropyl)- → HCID 22717494, compound
https://huagongshe.com/reaction/1582516
Participants
| Role | Name | HCID | Charge |
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| Reactant | Silane, chlorodimethyl(3,3,3-trifluoropropyl)- | HCID 73866 | — |
| Reactant | Tetrahydro-2-(2-propynyloxy)-2H-pyran | HCID 98609 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22717494 | HCID 22717494 | — |
Reaction Steps
A solution of n-butyllithium (12.0 ml, 30.0 mmol, 2.5 mol dm−3 in hexanes) was added dropwise to a stirred, cooled (−78° C.) solution of compound 1 (4.20 g, 30.0 mmol) in THF (80 ml) under an atmosphere of dry nitrogen. The reaction mixture was maintained at −78° C. for 1.5 h and a solution of chlorodimethyl-3,3,3-trifluoropropylsilane (5.72 g, 30.0 mmol) in THF (20 ml) added dropwise. The reaction mixture was allowed to warm to room temperature, washed with water and the organic layer extracted into ethyl acetate/hexane (3 times). The combined extracts were washed with brine, dried (MgSO4) and the solvent removed in vacuo to yield an amber oil. The crude product was purified by column chromatography [silica gel, eluted with hexane/ethyl acetate (4:1), Rf: 0.58] to yield a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06737124B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-1e97f0f366d94e9e9682ff2815cc031d |
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| Source note | uspto-grants-2004_05 |
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