Method for the prepration of aliphatic chloroformates
View Patent ↗A method for preparing an aliphatic chloroformate comprising, introducing a mixture of at least one aliphatic hydroxyl compound, phosgene, at least one solvent, and optionally at least one organic base into a flow reactor to obtain a unidirectional flowing reaction mixture. The at least one aliphatic hydroxyl compound comprises at least one aliphatic hydroxyl group. The unidirectional flowing reaction mixture is maintained at a temperature between about 0° C. and about 60° C. to produce a single product stream comprising an aliphatic chloroformate.
1. A method of preparing an aliphatic chloroformate, said method comprising:
(a) introducing into a flow reactor at least one aliphatic hydroxyl compound said aliphatic hydroxyl compound comprising at least one aliphatic hydroxyl group, phosgene, at least one solvent, and optionally an organic base to form a unidirectional flowing reaction mixture; and
(b) maintaining said unidirectional flowing reaction mixture at a temperature in a range between about 0° C. and about 60° C. to produce a product stream comprising an aliphatic chloroformate,
wherein only the product stream(s) exit the flow reactor.
2. The method according to claim 1 wherein said product stream is a single product stream.
3. The method according to claim 1 wherein said temperature is in a range between about 10° C. and about 50° C.
4. The method according to claim 1 wherein said unidirectional flowing reaction mixture is substantially anhydrous.
5. The method according to claim 1 wherein said flow reactor is a tubular reactor.
6. The method according to claim 1 wherein said aliphatic chloroformate comprises at least one chloroformate selected from the group consisting of monochloroformates, bischloroformates, trischloroformates, and polychloroformates.
7. The method according to claim 6 wherein said aliphatic chloroformate is a bischloroformate.
8. The method according to claim 1 wherein said unidirectional flowing reaction mixture is characterized by a molar ratio of phosgene to the aliphatic hydroxyl groups, said ratio being in a range of from about 1.1 to 1 to about 100 to 1.
9. The method according to claim 1 wherein said unidirectional flowing reaction mixture is characterized by a molar ratio of phosgene to the aliphatic hydroxyl groups, said ratio being in a range of from about 1.1 to 1 to about 4 to 1.
10. The method according to claim 1 wherein said solvent is selected from the group consisting of aliphatic solvents, and aromatic solvents.
11. The method according to claim 1 wherein said solvent is selected from the group consisting of chlorinated aliphatic solvents.
12. The method according to claim 11 wherein said solvent is methylene chloride.
13. The method according to claim 1 wherein said organic base is selected from the group consisting of amine bases and polyamine bases.
14. The method according to claim 1 wherein said unidirectional flowing reaction mixture is characterized by a molar ratio of the organic base to the aliphatic hydroxyl groups, said ratio being in a range of from about 0.01 to 1 to about 100 to 1.
15. The method according to claim 14 wherein said unidirectional flowing reaction mixture is characterized by a molar ratio of the organic base to the aliphatic hydroxyl groups, said ratio being in a range of from about 0.01 to 1 to about 5 to 1.
16. The method according to claim 14 wherein said unidirectional flowing reaction mixture is characterized by a molar ratio of the organic base to the aliphatic hydroxyl groups, said ratio being in a range of from about 0.01 to 1 to about 1.1 to 1.
17. The method according to claim 1 wherein said aliphatic hydroxyl compound comprises structural units having formula I
wherein R 1 and R 2 are independently at each occurrence a hydrogen atom, a C 1 -C 5 aliphatic radical, a C 3 -C 7 cycloaliphatic radical, an C 3 -C 6 aromatic radical, or R 1 and R 2 may together form a C 3 -C 6 cycloaliphatic radical; Q is a moiety having a total number of positions available for substitution and is a bond, a hydrogen atom, a C 1 -C 10 aliphatic radical, a C 3 -C 6 cycloaliphatic radical, or a C 3 -C 6 aromatic radical; and n is a number from 1 to the total number of positions on Q available for substitution.
18. The method according to claim 1 wherein said aliphatic hydroxyl compound is selected from the group consisting of aliphatic mono-alcohols and aliphatic polyols.
19. The method according to claim 1 wherein said aliphatic hydroxyl compound is selected from the group consisting of polymeric aliphatic hydroxyl compounds.