Process for the preparation of 2,3,3,3-tetrafluoropropene from methyl chloride and chlorodifluoromethane

A process for preparation of 2,3,3,3-tetrafluoropropene comprising:

• a) providing a mixture of methyl chloride to chlorodifluoromethane in first reactor, wherein said mixture is either premixed or added separately;
• b) providing and contacting the heat medium with step a) mixture to form second mixture comprising 2,3,3,3-tetrafluoropropene, methyl chloride and the fluorinated compounds having a boiling point in the range of −14 to −90° C.;
• c) drying second mixture of step b) to obtain anhydrous second mixture;
• d) subjecting the anhydrous second mixture of step c) to distillation to obtain anhydrous third mixture comprising methane, trifluoromethane, chlorotrifluoroethene, chlorodifluoromethane, tetrafluoroethyelene, vinylidene fluoride and difluoromethane and anhydrous fourth mixture comprising 2,3,3,3-tetrafluoropropene, methyl chloride, octafluorocyclobutane, chlorotrifluoroethyelene and tetrafluorochloroethane;
• e) contacting the anhydrous third mixture of step d) with molecular sieve of size 3 Å to 5 Å to obtain a fifth mixture, said mixture is free of difluoromethane;
• f) providing the fifth mixture and steam into a second reactor to obtain a second mixture;
• g) drying the second mixture to obtain anhydrous second mixture, alone or in combination with step c);
• h) subjecting the anhydrous second mixture of step g) to distillation to obtain anhydrous third mixture comprising methane, tetrafluoroethyelene, vinylidene fluoride and difluoromethane and anhydrous fourth mixture comprising 2,3,3,3-tetrafluoropropene, methyl chloride, octafluorocyclobutane, chlorotrifluoroethyelene and tetrafluorochloroethane, alone or in combination with step d);
• i) subjecting the anhydrous fourth mixture of step d) and/or step h) to distillation to obtain anhydrous sixth mixture comprising 2,3,3,3-tetrafluoropropene and methyl chloride, and another mixture comprising methyl chloride, octafluorocyclobutane, chlorotetrafluoroethane and tetrafluoroethane;
• j) contacting the anhydrous sixth mixture of step i) with molecular sieve of size 3 Å to 5 Å to obtain seventh mixture, said mixture is free of methyl chloride;
• and
• k) isolating 2,3,3,3-tetrafluoropropene from seventh mixture of step j).

A process for preparation of 2,3,3,3-tetrafluoropropene comprising:

• a) providing a mixture of methyl chloride to chlorodifluoromethane in a first reactor, said mixture is either premixed or added separately;
• b) providing and contacting heat medium with step a) mixture to form a second mixture comprising 2,3,3,3-tetrafluoropropene, methyl chloride and fluorinated compounds having a boiling point in the range of −14 to −90° C.;
• c) drying the second mixture of step b) to obtain an anhydrous second mixture;
• d) contacting the anhydrous second mixture of step c) with a solvent to obtain an anhydrous mixture 3′ in gas phase and anhydrous mixture 4′ in liquid phase, wherein the anhydrous mixture 3′ comprises methane, tetrafluoroethyelene, trifluoromethane, vinylidene fluoride, difluoromethane, chlorotrifluoroethene, hexafluoropropene, chlorodifluoromethane, 2,3,3,3-tetrafluoropropene, octafluorocyclobutane and methyl chloride and anhydrous mixture 4′ comprises solvent and methyl chloride;
• e) contacting the anhydrous mixture 3′ with 4 Å molecular sieves to obtain a mixture 5′, wherein the mixture 5′ is free of methyl chloride and difluoromethane;
• f) subjecting the anhydrous mixture 4′ of step d) to distillation to obtain a mixture 7′ comprising methyl chloride which is recycled into the existing reactor and mixture 8′ comprising solvent which is reused;
• g) subjecting the mixture 5′ of step e) to distillation to obtain a mixture 9′ comprising methane, tetrafluoroethyelene, trifluoromethane, vinylidene fluoride, hexafluoropropene and chlorodifluoromethane and a mixture 10′ comprising chlorotrifluoroethyelene, 2,3,3,3-tetrafluoropropene, octafluorocyclobutane, tetrafluorochloroethane and tetrafluoroethane;
• h) recycling mixture 9′ of step g) to the existing reactor or to the second reactor;
• i) subjecting the mixture 10′ of step g) to distillation to obtain a mixture 11′ comprising 2,3,3,3-tetrafluoropropene and chlorotrifluoroethyelene and a mixture 12′ comprising octafluorocyclobutane, chlorotetrafluoroethanes, tetrafluoroethane and heavies;
• j) subjecting the mixture 12′ of step i) to distillation to obtain a mixture 13′ comprising octafluorocyclobutane, chlorotetrafluoroethanes and tetrafluoroethanes which is recycled into reactor, and
• k) isolating 2,3,3,3-tetrafluoropropene from the mixture 11′.