Bimetallic catalyst for homogeneous methanol carhonylation and its prepn
A bimetallic catalyst, methanol carbonylation technology, applied in the direction of carbon monoxide reaction to prepare carboxylic acid, physical/chemical process catalyst, carbon monoxide or formate reaction preparation, etc., can solve the problem of increasing equipment corrosion
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0027] Weigh equimolar pyridine-2-carboxylic acid and lithium hydroxide and dissolve in methanol, reflux reaction for 1 hour under stirring, cool to room temperature, add dirhodium tetracarbonyl dichloride equivalent to 1 / 2 mole of pyridine-2-carboxylic acid , continue to stir for 20 minutes, add the sodium tetraphenylborate methanol solution with the same molar number as tetracarbonyl dirhodium dichloride, and react for ten minutes, precipitate with excess ether, and wash the lemon yellow precipitate twice with methanol at 0°C. Dry under reduced pressure at room temperature to constant weight to obtain a bidentate coordinated catalyst product.
Embodiment 2
[0029] Weigh equimolar pyridine-3-carboxylic acid and lithium hydroxide, dissolve in methanol, reflux reaction for 1 hour under stirring, cool to room temperature, add tetracarbonyl dichlorodichloride equivalent to 1 / 2 mole of pyridine-3-carboxylic acid Rhodium, continue to stir for 20 minutes, add sodium acetate methanol solution with the same molar number as tetracarbonyl dirhodium dichloride, after reacting for ten minutes, precipitate and filter with excess ether to obtain precipitate, wash twice with methanol at 0°C, and reduce to room temperature Press and dry to constant weight to obtain bidentate coordinated catalyst finished product.
Embodiment 3
[0031] Weigh equimolar pyridine-4-carboxylic acid and lithium hydroxide and dissolve them in methanol, reflux reaction for 1 hour under stirring, cool to room temperature, add dirhodium tetracarbonyl dichloride equivalent to 1 / 2 mole of pyridine-4-carboxylic acid , continue to stir for 20 minutes, use excess ether to precipitate, the precipitate is filtered, washed twice with methanol at 0°C, and dried under reduced pressure at room temperature to constant weight to obtain a finished monodentate coordinated catalyst.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More