Post-synthetic functionalization of porous materials
US-2024299905-A1 · Sep 12, 2024 · US
US12281059B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12281059-B2 |
| Application number | US-202117795207-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 21, 2021 |
| Priority date | Jan 27, 2020 |
| Publication date | Apr 22, 2025 |
| Grant date | Apr 22, 2025 |
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.
Provided is a method for producing a halogenated hydrocarbon magnesium compound, the method including bringing a halogenated hydrocarbon compound into contact with magnesium having a specific surface area of 1×10 −5 to 2×10 −4 m 2 /g. Also provided are methods for producing a tertiary alcohol compound and an organosilicon compound, wherein said production method is utilized.
Opening claim text (preview).
The invention claimed is: 1. A method for producing a halogenated hydrocarbon magnesium compound, the method comprising contacting a halogenated hydrocarbon compound with magnesium having a specific surface area of 1×10 −5 to 2×10 −4 m 2 /g. 2. The method for producing a halogenated hydrocarbon magnesium compound according to claim 1 , wherein the halogenated hydrocarbon compound is at least one selected from a mono-halogenated alkyl compound and a di-halogenated alkyl compound represented by the following formula (1): X—R—X (1) wherein R represents a linear or branched alkyl group having 1 to 8 carbon atoms and X represents a halogen atom. 3. The method for producing a halogenated hydrocarbon magnesium compound according to claim 1 , wherein the halogenated hydrocarbon compound is a hydrocarbon bromide compound. 4. The method for producing a halogenated hydrocarbon magnesium compound according to claim 1 , wherein the halogenated hydrocarbon compound is contacted with the magnesium at a temperature between −78° C. and 100° C. 5. The method for producing a halogenated hydrocarbon magnesium compound according to claim 1 , wherein a solution containing the halogenated hydrocarbon compound is contacted with the magnesium. 6. The method for producing a halogenated hydrocarbon magnesium compound according to claim 5 , wherein the solution containing the halogenated hydrocarbon compound is passed through a packed tower filled with the magnesium. 7. The method for producing a halogenated hydrocarbon magnesium compound according to claim 6 , wherein the solution containing the halogenated hydrocarbon compound is repeatedly passed through the packed tower filled with the magnesium. 8. The method for producing a halogenated hydrocarbon magnesium compound according to claim 6 , wherein a plurality of packed towers each filled with the magnesium exist and the solution containing the halogenated hydrocarbon compound is passed through the plurality of packed towers. 9. The method for producing a halogenated hydrocarbon magnesium compound according to claim 6 , wherein the solution containing the halogenated hydrocarbon compound has a temperature between −78° C. and 100° C. 10. A method for producing a tertiary alcohol compound, comprising: producing a halogenated hydrocarbon magnesium compound by the method according to claim 1 , and contacting the halogenated hydrocarbon magnesium compound with a ketone compound. 11. A method for producing an organosilicon compound, comprising: producing a halogenated hydrocarbon magnesium compound by the production method according to claim 1 , and contacting the halogenated hydrocarbon magnesium compound with a silicon compound selected from a chlorosilane compound and an alkoxysilane compound.
Related publications grouped by family.
Answers are generated from the same data shown on this page.