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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408492Generated: November 2, 2026

1H,1H,2H,2H-Perfluorooctyldimethylchlorosilane → HCID 86663263, compound

https://huagongshe.com/reaction/1408492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H,1H,2H,2H-PerfluorooctyldimethylchlorosilaneHCID 145382—
ReactantHCID 178418486HCID 178418486—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86663263HCID 8666326396%

Reaction Conditions

Temperature60 °C

Reaction Steps

In an oven-dried 250-mL round bottom flask, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyldimethylchlorosilane (9.67 g, 21.9 mmol) was dissolved in 20 mL anhydrous THF. Ethynylmagnesium bromide (50 mL, 25 mmol, 0.5 M in THF) was added and the mixture was heated to 60° C. for 12 hr. After allowing the mixture to cool to room temperature, the reaction was quenched by the dropwise addition of water, followed by the addition of dilute sulfuric acid to dissolve the magnesium salts. The organic layer was separated, washed with water (3×20 mL) and brine, dried over magnesium sulfate, filtered and concentrated under vacuum. The crude product was purified by chromatography on silica gel using hexane as an eluant. Removal of solvent yielded 9.0 g (21 mmol, 96%) of the product as a colorless liquid. Analysis of the colorless product provided the following data: 1H-NMR (200 MHz, CDCl3) δ=2.4 (s, 1H), 2.1 (m, 2H), 0.8 (m, 2H), 0.2 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08920679B2
Source datasetuspto-grants-2014_12
ORD IDord-84dc760a22074a3cb7c86cf1c2fbcbc4
Source noteuspto-grants-2014_12