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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSilane, chlorodimethyl(3,3,3-trifluoropropyl)-HCID 73866—
ReactantTetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22717494HCID 22717494—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737124B2
Source datasetuspto-grants-2004_05
ORD IDord-1e97f0f366d94e9e9682ff2815cc031d
Source noteuspto-grants-2004_05