Fluorosilicon nitrile compounds
US-2018370995-A1 · Dec 27, 2018 · US
US10590150B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10590150-B2 |
| Application number | US-201816057886-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 8, 2018 |
| Priority date | Aug 27, 2014 |
| Publication date | Mar 17, 2020 |
| Grant date | Mar 17, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Methods of synthesizing fluorosilanes containing cyano-substituted alkyl groups are provided. For example, 3-cyanopropyldimethylfluorosilane may be produced by reacting tetramethyldisiloxane and boron trifluoride to obtain fluorodimethylsilane and then reacting the fluorodimethylsilane with allyl cyanide, in the presence of a hydrosilylation catalyst.
Opening claim text (preview).
What is claimed is: 1. A method of making 3-cyanopropyldimethylfluorosilane comprising a step of reacting bis(3-cyanopropyl)tetramethyldisiloxane and boron trifluoride in an inert solvent capable of forming an azeotrope with water. 2. The method of claim 1 , wherein the boron trifluoride is in the form of an etherate complex. 3. The method of claim 1 , wherein the boron trifluoride and the bis(cyanopropyl)tetramethyldisiloxane are reacted at a temperature of from about 60° C. to about 100° C. 4. The method of claim 1 , wherein the boron trifluoride and the bis(cyanopropyl)tetramethyldisiloxane are reacted at a molar ratio of from about 0.3:1 to about 1:1. 5. The method of claim 1 , wherein a reaction product containing 3-cyanopropyldimethylfluorosilane, inert solvent and water is obtained and the reaction product is subjected to distillation wherein water is removed by azeotropic distillation. 6. The method of claim 1 , wherein the inert solvent is an aromatic hydrocarbon. 7. The method of claim 6 , wherein the inert solvent is toluene.
by reactions involving both Si-C and Si-halogen linkages, the Si-C and Si-halogen linkages can be to the same or to different Si atoms, e.g. redistribution reactions · CPC title
by reactions involving the formation of Si-halogen linkages · CPC title
Preparation thereof from {optionally substituted} halogenated silanes and hydrocarbons {hydrosilylation reactions} · CPC title
Organo silicon halides · CPC title
by reactions involving the formation of Si-C linkages (hydrosilylation reactions C07F7/14; direct synthesis C07F7/16) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.