46117-43-5Relevant academic research and scientific papers
Synthesis of vinyl carbonates for use in producing vinyl carbamates
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Example 3, (2008/06/13)
A method for making a vinyl carbonate represented by the formula (I): CH2═CHOC(O)X1R1??(I) wherein X1is oxygen or sulfur and R1is a substituted or an unsubstituted aliphatic alkyl, aryl, aryl alkyl, olefinic, vinyl, or cycloaliphatic group comprises: (a) reacting a compound represented by the formula (II): X2C(O)X1R1??(II) ?wherein X2is a halogen other than fluorine, with a compound represented by the formula (III): M1—F??(III) ?wherein M1is selected from a Group IA metal, in the presence of a first phase transfer catalyst and a first organic solvent, to form a compound represented by the formula (IV): FC(O)X1R1??(IV) and (b) reacting a compound represented by the formula (IV) with a compound represented by the formula (V): CH2═CHOSi(R2)3??(V) ?wherein R2is a substituted or an unsubstituted aliphatic alkyl, aryl, aryl alkyl olefinic, vinyl, or cycloaliphatic group, or any combination thereof, in the presence of a metal salt represented by the formula M2—F wherein M2is a Group IA metal, a second phase transfer catalyst, and a second organic solvent, to form the compound represented by formula (I).
Synthesis of vinyl carbonates for use in producing vinyl carbamates
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, (2008/06/13)
A method for making a vinyl carbonate represented by the formula (I): CH2═CHOC(O)X1R1??(I) wherein X1is oxygen or sulfur and R1is a substituted or an unsubstituted aliphatic alkyl, aryl, aryl alkyl, olefinic, vinyl, or cycloaliphatic group comprises: (a) reacting a compound represented by the formula (II): X2C(O)X1R1??(II) wherein X2is a halogen other than fluorine, with a compound represented by the formula (III): M1—F??(III) wherein M1is selected from a Group IA metal, in the presence of a first phase transfer catalyst and a first organic solvent, to form a compound represented by the formula (IV): FC(O)X1R1??(IV); ?and (b) reacting a compound represented by the formula (IV) with a compound represented by the formula (V): CH2═CHOSi(R2)3??(V) wherein R2is a substituted or an unsubstituted aliphatic alkyl, aryl, aryl alkyl olefinic, vinyl, or cycloaliphatic group, or any combination thereof, in the presence of a metal salt represented by the formula M2—F wherein M2is a Group IA metal, a second phase transfer catalyst, and a second organic solvent, to form the compound represented by formula (I).
