Method for efficiently preparing benzaldehyde by using air as oxidation agent to catalyze benzyl alcohol in alkali-free water phase system at room temperature
A technology of oxidant and benzyl alcohol, which is applied in the direction of catalyst activation/preparation, heterogeneous catalyst chemical elements, metal/metal oxide/metal hydroxide catalyst, etc., can solve the problem of low selectivity and achieve simple reaction process, The effect of mild reaction conditions and high application prospects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0035] (1) Dissolve chloroplatinic acid hexahydrate in deionized water to make the concentration of Pt element 19.2 mM, and ultrasonicate for 5 minutes until the soluble Pt salt is completely dissolved to obtain a yellow transparent solution A;
[0036] (2) Disperse 0.5 g of ZnO in 10 mL of deionized water, and ultrasonically disperse the metal oxide for 5 minutes to obtain suspension B;
[0037] (3) Under stirring conditions, add 1.66 mL of A solution to B to obtain a light yellow mixture C. The mass ratio of Pt element to ZnO is 1:100;
[0038] (4) Dissolve 30 mg of sodium borohydride in 6 mL of ice water, and sonicate for 5 min to form a colorless and transparent solution D;
[0039] (5) After stirring the above mixture C for 1 hour, slowly add solution D dropwise to it, so that the molar ratio of the Pt element in the mixture C to the sodium borohydride added dropwise is 1:5, to obtain a gray-brown suspension emulsion E ;
[0040] (6) After the suspension emulsion E was stirred for...
Embodiment 2
[0043] (1) Dissolve chloroplatinic acid hexahydrate in deionized water to make the concentration of Pt element 19.2 mM, and ultrasonicate for 5 minutes until the soluble Pt salt is completely dissolved to obtain a yellow transparent solution A;
[0044] (2) Disperse 0.5 g of ZnO in 10 mL of deionized water, and ultrasonically disperse the metal oxide for 5 minutes to obtain suspension B;
[0045] (3) Under stirring conditions, add 1.66 mL of A solution to B to obtain a light yellow mixture C. The mass ratio of Pt element to ZnO is 1:100;
[0046] (4) Dissolve 30 mg of sodium borohydride in 10 mL of ice water, and sonicate for 5 minutes to form a colorless and transparent solution D;
[0047] (5) After stirring the above mixture C for 1 hour, slowly add solution D dropwise to it, so that the molar ratio of the Pt element in the mixture C to the sodium borohydride added dropwise is 1:5, to obtain a gray-brown suspension emulsion E ;
[0048] (6) After the suspension emulsion E was stirre...
Embodiment 3
[0051] (1) Dissolve chloroplatinic acid hexahydrate in deionized water to make the concentration of Pt element 19.2 mM, and ultrasonicate for 5 minutes until the soluble Pt salt is completely dissolved to obtain a yellow transparent solution A;
[0052] (2) Disperse 0.5 g of ZnO in 10 mL of deionized water, and ultrasonically disperse the metal oxide for 5 minutes to obtain suspension B;
[0053] (3) Under stirring conditions, add 1.66 mL of A solution to B to obtain a light yellow mixture C. The mass ratio of Pt element to ZnO is 1:100;
[0054] (4) Dissolve 30 mg of sodium borohydride in 6 mL of ice water, and sonicate for 5 min to form a colorless and transparent solution D;
[0055] (5) After stirring the above mixture C for 1 hour, slowly add solution D dropwise to it, so that the molar ratio of the Pt element in the mixture C to the sodium borohydride added dropwise is 1:5, to obtain a gray-brown suspension emulsion E ;
[0056] (6) After the suspension emulsion E was stirred for...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com