Process for the preparation of highly purified, dialkyl phosphinic acids
View Patent ↗In a process for the production of dialkylphosphinic acids, especially branched, dialkylphosphinic acids in high purity via the reaction of an alpha olefin with a hypophosphorous acid or a salt thereof, the improvement comprising conducting the reaction in the presence of a stoichiometric excess of the olefin and isolating and purifying the desired dialkylphosphinic acid product by neutralizing the monoalkylphosphinic acid by-product with an aqueous base; removing the aqueous phase in which the neutralized monoalkylphosphinic acid is preferentially solubilized; acidifying the dialkyl product in the organic phase; and isolating the purified product.
1. An improved process for the production of dialkylphosphinic acid in high yield and purity by the reaction of a hypophosphorous acid or salt with a stoichiometric excess of an alpha olefin in the presence of a free radical initiator and optionally a transition metal catalyst to form a reaction product composition comprising monoalkylphosphinic acid and dialkylphosphinic acid; the improvement comprising:
a) adding sufficient aqueous base to the reaction product composition to i) form the salts of the phosphinic acids, and ii) establish an aqueous phase and an organic phase, wherein the monoalkylphosphinic acid preferentially solubilizes into the aqueous phase;
b) separating the organic phase from the aqueous phase;
c) acidifying the organic phase; and
d) removing the olefin from the organic phase; and
e) isolating the purified dialkylphosphinic acid product.
2. The process of claim 1 wherein the dialkylphosphinic acid is of the following formula:
wherein R 1 and R 2 are each independently an alkyl radical having from 2 to 22 carbon atoms.
3. The process of claim 2 wherein R 1 and R 2 are each independently a substituted alkyl radical having from 2 to 12 carbon atoms.
4. The process of claim 3 wherein the R 1 and R 2 are each independently a substituted alkyl radical having from 2 to 9 carbon atoms.
5. The process of claim 2 wherein the alkyl radicals are each independently substituted by two or more radicals selected from the group consisting of chloro-, bromo, alkyl, alkoxy groups and mixtures thereof.
6. The process of claim 3 wherein the alkyl radicals are each independently substituted by two or more radicals selected from the group consisting of chloro-, bromo, alkyl, alkoxy groups and mixtures thereof.
7. The process of claim 4 wherein the alkyl radicals are each independently substituted by two or more radicals selected from the group consisting of chloro-, bromo, alkyl, alkoxy groups and mixtures thereof.
8. The process of claim 1 wherein the reaction to form the reaction product composition takes place in the presence of an acid solution.
9. The process of claim 8 wherein the acid solution is selected from the group consisting of hydrochloric acid, sulfuric acid, acetic acid and mixtures thereof.
10. The process of claim 9 wherein the acid solution is an acetic acid solution.
11. The process of claim 1 wherein the hypophosphorous salt is sodium hypophosphite monohydrate.
12. The process of claim 1 wherein the molar ratio of the alpha olefin to the hypophosphorous acid or salt is greater than 2:1.
13. The process of claim 12 wherein the molar ratio of the alpha olefin to the hypophosphorous acid or salt is greater than 2.5 to 1.
14. The process of claim 1 wherein the aqueous base which is added to the reaction product composition is an aqueous sodium hydroxide solution or an aqueous sodium carbonate solution.
15. The process of claim 1 wherein the acid in the acidification step comprises an inorganic acid solution.
16. The process of claim 15 wherein the inorganic acid solution is a sulfuric acid solution.
17. The process of claim 1 wherein the olefin removed is recycled.