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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H,1H,2H,2H-Perfluorooctyldimethylchlorosilane | HCID 145382 | — |
| Reactant | HCID 178418486 | HCID 178418486 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86663263 | HCID 86663263 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08920679B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-84dc760a22074a3cb7c86cf1c2fbcbc4 |
|---|
| Source note | uspto-grants-2014_12 |
|---|