Patent classifications
C07C29/38
PROCESS FOR PREPARING AN UNSATURATED ALCOHOL
The present invention relates to a process for preparing an unsaturated alcohol, preferably 3,7-dimethyl-2,6-octadienal, by contacting an alkene, preferably isobutene, with formaldehyde in the presence a condensation catalyst comprising a zeolitic material comprising the framework structure of which comprises a tetravalent element Y other than Si.
SYNTHESIS OF SODIUM FORMATE AND DRILLING FLUID COMPRISING THE SAME
A method of synthesizing sodium formate. The method includes reacting acetaldehyde, formaldehyde, and NaOH to form a raw reaction solution which includes pentaerythritol and sodium formate. The method also includes passing the raw reaction solution to an evaporator to reduce the water content of the raw reaction solution and remove any unreacted formaldehyde from the raw reaction solution to form a concentrated reaction solution and cooling the concentrated reaction solution to form pentaerythritol crystals in suspension while retaining sodium formate in solution. Further, the method includes filtering the cooled concentrated reaction solution to remove the pentaerythritol crystals and create a mother liquor comprising the sodium formate in solution and separating the sodium formate from the mother liquor.
SYNTHESIS OF SODIUM FORMATE AND DRILLING FLUID COMPRISING THE SAME
A method of synthesizing sodium formate. The method includes reacting acetaldehyde, formaldehyde, and NaOH to form a raw reaction solution which includes pentaerythritol and sodium formate. The method also includes passing the raw reaction solution to an evaporator to reduce the water content of the raw reaction solution and remove any unreacted formaldehyde from the raw reaction solution to form a concentrated reaction solution and cooling the concentrated reaction solution to form pentaerythritol crystals in suspension while retaining sodium formate in solution. Further, the method includes filtering the cooled concentrated reaction solution to remove the pentaerythritol crystals and create a mother liquor comprising the sodium formate in solution and separating the sodium formate from the mother liquor.
SYNTHESIS OF SODIUM FORMATE AND DRILLING FLUID COMPRISING THE SAME
A method of synthesizing sodium formate. The method includes reacting acetaldehyde, formaldehyde, and NaOH to form a raw reaction solution which includes pentaerythritol and sodium formate. The method also includes passing the raw reaction solution to an evaporator to reduce the water content of the raw reaction solution and remove any unreacted formaldehyde from the raw reaction solution to form a concentrated reaction solution and cooling the concentrated reaction solution to form pentaerythritol crystals in suspension while retaining sodium formate in solution. Further, the method includes filtering the cooled concentrated reaction solution to remove the pentaerythritol crystals and create a mother liquor comprising the sodium formate in solution and separating the sodium formate from the mother liquor.
SYNTHESIS OF SODIUM FORMATE AND DRILLING FLUID COMPRISING THE SAME
A method of synthesizing sodium formate. The method includes reacting acetaldehyde, formaldehyde, and NaOH to form a raw reaction solution which includes pentaerythritol and sodium formate. The method also includes passing the raw reaction solution to an evaporator to reduce the water content of the raw reaction solution and remove any unreacted formaldehyde from the raw reaction solution to form a concentrated reaction solution and cooling the concentrated reaction solution to form pentaerythritol crystals in suspension while retaining sodium formate in solution. Further, the method includes filtering the cooled concentrated reaction solution to remove the pentaerythritol crystals and create a mother liquor comprising the sodium formate in solution and separating the sodium formate from the mother liquor.
Processes for preparing vinylidene dimer derivatives
This disclosure provides a process for producing vinylidene dimer derivatives by subjecting one or more vinylidene dimers and one or more carbonyl-containing compounds to a carbonyl-ene reaction, optionally in the presence of a catalyst, to produce one or more vinylidene dimer derived alcohols. This disclosure also provides a process for producing vinylidene dimer derivatives by reacting one or more vinylidene dimers with one or more carbonyl-containing compounds, optionally in the presence of a catalyst, to produce one or more vinylidene dimer derived alcohols. This disclosure further provides vinylidene dimer derivatives (e.g., vinylidene dimer derived alcohols and esters) produced by these processes. This disclosure still further provides for hydrogenating/reacting the vinylidene dimer derived alcohols with acids or anhydrides to produce vinylidene dimer derived esters. This disclosure yet further relates to lubricating ester oil base stocks, and lubricating oils containing the lubricating ester oil base stocks.
Processes for preparing vinylidene dimer derivatives
This disclosure provides a process for producing vinylidene dimer derivatives by subjecting one or more vinylidene dimers and one or more carbonyl-containing compounds to a carbonyl-ene reaction, optionally in the presence of a catalyst, to produce one or more vinylidene dimer derived alcohols. This disclosure also provides a process for producing vinylidene dimer derivatives by reacting one or more vinylidene dimers with one or more carbonyl-containing compounds, optionally in the presence of a catalyst, to produce one or more vinylidene dimer derived alcohols. This disclosure further provides vinylidene dimer derivatives (e.g., vinylidene dimer derived alcohols and esters) produced by these processes. This disclosure still further provides for hydrogenating/reacting the vinylidene dimer derived alcohols with acids or anhydrides to produce vinylidene dimer derived esters. This disclosure yet further relates to lubricating ester oil base stocks, and lubricating oils containing the lubricating ester oil base stocks.
Preparation process of perfluoroalkyl compound with monohydroperfluoroalkane as starting material
A simple production process is provided of a perfluoroalkyl compound that uses monohydroperfluoroalkane as a starting material, the perfluoroalkyl compound being an important intermediate of organic electronic materials, medicine, agricultural chemicals, functional polymer materials and the like. With monohydroperfluoroalkane is reacted a base and then a carbonyl compound to produce an alcohol having a perfluoroalkyl group. For example, potassium hydroxide is made to interact with trifluoromethane, and a reaction with a carbonyl compound is induced to produce an alcohol having a trifluoromethyl group.
Preparation process of perfluoroalkyl compound with monohydroperfluoroalkane as starting material
A simple production process is provided of a perfluoroalkyl compound that uses monohydroperfluoroalkane as a starting material, the perfluoroalkyl compound being an important intermediate of organic electronic materials, medicine, agricultural chemicals, functional polymer materials and the like. With monohydroperfluoroalkane is reacted a base and then a carbonyl compound to produce an alcohol having a perfluoroalkyl group. For example, potassium hydroxide is made to interact with trifluoromethane, and a reaction with a carbonyl compound is induced to produce an alcohol having a trifluoromethyl group.
Preparation process of perfluoroalkyl compound with monohydroperfluoroalkane as starting material
A simple production process is provided of a perfluoroalkyl compound that uses monohydroperfluoroalkane as a starting material, the perfluoroalkyl compound being an important intermediate of organic electronic materials, medicine, agricultural chemicals, functional polymer materials and the like. With monohydroperfluoroalkane is reacted a base and then a carbonyl compound to produce an alcohol having a perfluoroalkyl group. For example, potassium hydroxide is made to interact with trifluoromethane, and a reaction with a carbonyl compound is induced to produce an alcohol having a trifluoromethyl group.