Method for the preparation of aromatic chloroformates
View Patent ↗A method for preparing an aromatic chloroformate comprising, introducing a mixture of at least one aromatic hydroxyl compound, phosgene, at least one solvent, and at least one organic base into a flow reactor to obtain a unidirectionally flowing reaction mixture. The unidirectionally flowing reaction mixture is maintained at a temperature between about 0° C. and about 60° C. to produce a single product stream comprising an aromatic chloroformate.
1. A method of preparing an aromatic chloroformate, said method comprising:
(a) introducing into a flow reactor at least one aromatic hydroxyl compound, phosgene, at least one solvent, and at least one organic base to form a unidirectionally flowing reaction mixture, said unidirectionally flowing reaction mixture being substantially free of water; and
(b) maintaining said unidirectionally flowing reaction mixture at a temperature in a range between about 0° C. and about 60° C. to produce a product stream comprising an aromatic chloroformate.
2. The method according to claim 1 wherein said aromatic hydroxyl compound comprises structural units having formula I
(R) m -Q-(OH) n Formula I
wherein Q is a C 3 -C 20 aromatic radical, R is independently at each occurrence a hydrogen atom, a C 1 -C 5 aliphatic radical, a C 3 -C 7 cycloaliphatic radical or a C 3 -C 6 aromatic radical, “n” is a number equal to the total number of aromatic positions on Q available for substitution and “m” is an integer having value 0 to {(the total number of positions on Q available for substitution)-n }.
3. The method according to claim 1 wherein said aromatic chloroformate comprises at least one chloroformate selected from the group consisting of monochloroformates, bischloroformates, trischloroformates, and polychlororformates.
4. The method according to claim 3 wherein said aromatic chloroformate is a monochloroformate.
5. The method according to claim 1 wherein said unidirectionally flowing reaction mixture comprises less than 1% by weight water.
6. The method according to claim 1 wherein said solvent is selected from the group consisting of aliphatic solvents and aromatic solvents.
7. The method according to claim 6 wherein said solvent is selected from the group consisting of chlorinated aliphatic solvents.
8. The method according to claim 7 wherein said solvent is methylene chloride.
9. The method according to claim 1 wherein said organic base is selected from the group consisting of amine bases and polyamine bases.
10. The method according to claim 1 wherein said unidirectionally flowing reaction mixture is characterized by a molar ratio of phosgene to the aromatic hydroxyl groups, said ratio being in a range of from about 1.1 to about 100 to 1.
11. The method according to claim 10 wherein said unidirectionally flowing reaction mixture is characterized by a molar ratio of phosgene to the aromatic hydroxyl groups, said ratio being in a range of from about 1.1 to about 5 to 1.
12. The method according to claim 1 wherein said unidirectionally flowing reaction mixture is characterized by a molar ratio of the organic base to the aromatic hydroxyl groups, said ratio being in a range of from about 0.01 to about 100 to 1.
13. The method according to claim 12 wherein said unidirectionally flowing reaction mixture is characterized by a molar ratio of the organic base to the aromatic hydroxyl groups, said ratio being in a range of from about 0.01 to 1 to about 5 to 1.
14. The method according to claim 13 wherein said unidirectionally flowing reaction mixture is characterized by a molar ratio of the organic base to the aromatic hydroxyl groups, said ratio being in a range of from about 0.01 to about 1.1 to 1.
15. The method according to claim 1 wherein said product stream is a single product stream.
16. The method according to claim 1 wherein said temperature is in a range between about 10° C. and about 50° C.
17. The method according to claim 1 wherein said flow reactor is a tubular reactor.
18. A method for preparing a co-polycarbonate said method comprising reacting at least one dihydroxy aromatic compound under interfacial conditions with phosgene and an aromatic chloroformate, said aromatic chloroformate being prepared by a method comprising;
(a) introducing into a flow reactor at least one aromatic hydroxyl compound, phosgene, at least one solvent, and an organic base to form a unidirectionally flowing reaction mixture, said unidirectionally flowing reaction mixture being substantially free of water; and
(b) maintaining said unidirectionally flowing reaction mixture at a temperature in a range between about 0° C. and about 60° C. to produce a product stream comprising an aromatic chloroformate.
19. The method according to claim 18 wherein the aromatic chloroformate product from the flow reactor is used in its entirety and without purification.
20. The method according to claim 18 wherein said dihydroxy aromatic compound is a bisphenol having formula II;
wherein each G 1 is independently at each occurrence a C 6 -C 20 aromatic radical; E is independently at each occurrence a bond, a C 3 -C 20 cycloaliphatic radical, a C 6 -C 20 aromatic radical, a C 1 -C 20 aliphatic radical, a sulfur-containing linkage, a selenium-containing linkage, a phosphorus-containing linkage, or an oxygen atom; “t” is a number greater than or equal to one; “s” is either zero or one; and “u” is a whole number including zero.
21. A method of preparing an aromatic chloroformate, said method comprising:
(a) introducing into a flow reactor at least one aromatic hydroxyl compound, phosgene, at least one solvent, and an organic base to form a unidirectionally flowing reaction mixture, said unidirectionally flowing reaction mixture being substantially free of water; and
(b) maintaining said unidirectionally flowing reaction mixture at a temperature in a range between about 0° C. and about 60° C. to produce a product stream comprising an aromatic chloroformate;
wherein said aromatic hydroxyl compound is not a aromatic hydroxyl compound comprising only hydroxyl groups flanked on each side by tertiary aliphatic and/or tertiary cycloaliphatic radicals.
22. A method of preparing an aromatic chloroformate, said method comprising:
(a) introducing into a flow reactor at least one aromatic hydroxyl compound, phosgene, at least one solvent, and at least one organic base to form a unidirectionally flowing reaction mixture, said unidirectionally flowing reaction mixture being substantially free of water, wherein said aromatic hydroxyl compound has formula III;
wherein R is independently at each occurrence a hydrogen atom, a C 1 -C 25 aliphatic radical, a C 3 -C 20 cycloaliphatic radical or a C 3 -C 20 aromatic radical, and “m” is an integer having value 0 to 5, and wherein said aromatic hydroxyl compound is not a mono-hydroxy aromatic compound in which the hydroxyl group of formula III is flanked on each side by tertiary aliphatic and/or tertiary cycloaliphatic radicals; and
(b) maintaining said unidirectionally flowing reaction mixture at a temperature in a range between about 0° C. and about 60° C. to produce a product stream comprising an aromatic chloroformate.