A kind of preparation method of liquid carbon dioxide thickener
A liquid carbon dioxide and thickener technology, applied in the preparation of organic compounds, chemical instruments and methods, preparation of urea derivatives, etc., can solve problems such as reservoir damage, impact on fracturing stimulation, and reduction of reservoir permeability Effect of increasing viscosity and improving dissolution
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0018] (1) Preparation of 1,3-dihydroxypropane-2-carbamic acid tert-butyl ester
[0019] Add 6mL of deionized water and 14mL of methanol into the three-necked flask, stir and mix evenly, then add 0.02mol of serinol into the mixed solution, stir to dissolve completely, cool down to 0°C with an ice bath, and then add the three to the mixed solution Slowly add 0.022mol of di-tert-butyl dicarbonate dropwise. During the dropping process, the temperature was kept at 0°C. After 30 minutes, the ice bath was removed, and the reaction was carried out at a constant temperature of 25°C for 4 hours. After the reaction was completed, it was extracted three times with dichloromethane. The solvent methanol and water were distilled off under reduced pressure, and vacuum-dried at 45° C. for 24 hours to obtain the product tert-butyl 1,3-dihydroxypropane-2-carbamate.
[0020] (2) Preparation of perfluorooctanoyl chloride
[0021] Add 0.02mol of perfluorooctanoic acid into another three-necked fl...
Embodiment 2
[0027] (1) Preparation of 1,3-dihydroxypropane-2-carbamic acid tert-butyl ester
[0028] Add 6mL of deionized water and 14mL of methanol into the three-necked flask, stir to dissolve completely, and cool down to 0°C with an ice bath, then slowly add 0.021mol of di-tert-butyl dicarbonate dropwise to the mixed solution of the three, during the dropwise addition , the temperature was kept at 0°C. After 30 minutes, the ice bath was removed, and the reaction was carried out at a constant temperature of 25°C for 4 hours. After the reaction was completed, the solvents methanol and water were distilled off under reduced pressure after extraction with dichloromethane three times, and dried in vacuum at 45°C. After 24h, the product tert-butyl 1,3-dihydroxypropane-2-carbamate was obtained.
[0029] (2) Preparation of perfluorooctanoyl chloride
[0030] Take 0.02mol of perfluorooctanoic acid and add it to another three-necked flask equipped with a condenser, raise the temperature to 75°C...
Embodiment 3
[0036] (1) Preparation of 1,3-dihydroxypropane-2-carbamic acid tert-butyl ester
[0037] Add 6mL of deionized water and 14mL of methanol into the three-necked flask, stir and mix evenly, take 0.02mol of serinol and add it into the mixed solution, stir to dissolve completely, cool down to 0°C with an ice bath, and then slowly add to the mixed solution of the three. Add 0.023mol of di-tert-butyl dicarbonate dropwise. During the dropwise addition, the temperature was kept at 0°C. After 30 minutes, the ice bath was removed, and the reaction was carried out at a constant temperature of 25°C for 4 hours. The solvent methanol and water were distilled off under pressure, and vacuum-dried at 45°C for 24 hours to obtain the intermediate product 1,3-dihydroxypropane-2-carbamate tert-butyl ester.
[0038] (2) Preparation of perfluorooctanoyl chloride
[0039] Take 0.02mol of perfluorooctanoic acid and add it into another three-necked flask equipped with a condenser, raise the temperature...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


