Method for producing a (meth)acrylate
View Patent ↗Disclosed is a method for producing a (meth)acrylate ester wherein a high purity (meth)acrylate ester is obtained with a high yield, with a reduced loss of (meth)acrylic acid anhydride. In the method, (meth)acrylic acid is recovered with a high yield, and the (meth)acrylate ester is purified easily. Specifically disclosed is a method for producing a (meth)acrylate ester which comprises: (1) a step of producing (meth)acrylic acid anhydride by reacting a specific fatty acid anhydride and (meth)acrylic acid, while removing a by-produced fatty acid; (2) a step of obtaining a (meth)acrylate ester by reacting an alcohol and unpurified (meth)acrylic acid anhydride obtained in step (1) preferably at a temperature not less than 90° C.; and (3) a step of recovering (meth)acrylic acid by distillation preferably at a temperature not less than 90° C. The method may also comprise a step of heating or distilling the reaction liquid obtained in step (2) at a temperature not less than 90° C.
1. A method for producing a (meth)acrylate, the method comprising:
(1) producing (meth)acrylic acid anhydride, comprising reacting a fatty acid anhydride of formula (I)
wherein
R 1 is a linear or branched, alkyl group or alkenyl group, having a carbon number 1 to 3, and
R 2 is a linear or branched alkyl group having a carbon number 1 to 3,
with (meth)acrylic acid to produce (meth)acrylic acid anhydride, while extracting a fatty acid produced as a by-product;
(2) obtaining the (meth)acrylate by reacting a phenol with crude (meth)acrylic acid anhydride obtained by the producing (1), wherein the obtaining (2) is carried out at a temperature in a range of 90° C. or more and 120° C. or less; and
(3) recovering (meth)acrylic acid by distillation.
2. A method for producing a (meth)acrylate, the method comprising:
(1) producing (meth)acrylic acid anhydride, comprising reacting a fatty acid anhydride of formula (I)
wherein
R 1 is a linear or branched, alkyl group or alkenyl group, having a carbon number 1 to 3, and
R 2 is a linear or branched alkyl group having a carbon number 1 to 3,
with (meth)acrylic acid to produce (meth)acrylic acid anhydride, while extracting a fatty acid produced as a by-product;
(2) obtaining the (meth)acrylate by reacting a phenol with crude (meth)acrylic acid anhydride obtained by the producing (1); and
(3) recovering (meth)acrylic acid by distillation at a temperature in a range of 90° C. or more and 130° C. or less.
3. A method for producing a (meth)acrylate, the method comprising:
(1) producing (meth)acrylic acid anhydride, comprising reacting a fatty acid anhydride of formula (I)
wherein
R 1 is a linear or branched, alkyl group or alkenyl group, having a carbon number 1 to 3, and
R 2 is a linear or branched alkyl group having a carbon number 1 to 3,
with (meth)acrylic acid to produce (meth)acrylic acid anhydride, while extracting a fatty acid produced as a by-product;
(2) obtaining the (meth)acrylate by reacting a phenol with crude (meth)acrylic acid anhydride obtained by the producing (1);
(2′) heating the reaction liquid obtained by the obtaining (2) at a temperature in the range of 90° C. or more and 130° C. or less; and
(3) recovering (meth)acrylic acid by distillation.
4. A method for producing a (meth)acrylate, the method comprising:
(1) producing (meth)acrylic acid anhydride, comprising reacting a fatty acid anhydride of formula (I)
wherein
R 1 is a linear or branched, alkyl group or alkenyl group, having a carbon number 1 to 3, and
R 2 is a linear or branched alkyl group having a carbon number 1 to 3,
with (meth)acrylic acid to produce (meth)acrylic acid anhydride, while extracting a fatty acid produced as a by-product;
(2) obtaining the (meth)acrylate by reacting a phenol with crude (meth)acrylic acid anhydride obtained by the producing (1);
(2″) obtaining a reaction liquid containing (meth)acrylic acid and the (meth)acrylate by distillation of the reaction liquid obtained by the obtaining (2) at a temperature in a range of 90° C. or more and 130° C. or less; and
(3) recovering (meth)acrylic acid by distillation.
5. The method of claim 1 , wherein the (meth)acrylic acid anhydride remaining in a reaction liquid obtained by the obtaining (2) is hydrolyzed by addition of at least one basic compound selected from the group consisting of a hydroxide, a carbonate, a bicarbonate, and an oxide of at least one selected from the group consisting of an alkali metal and an alkaline earth metal to a reaction liquid obtained by the obtaining (2).
6. The method of claim 2 , wherein the (meth)acrylic acid anhydride remaining in a reaction liquid obtained by the obtaining (2) is hydrolyzed by addition of at least one basic compound selected from the group consisting of a hydroxide, a carbonate, a bicarbonate, and an oxide of at least one selected from the group consisting of an alkali metal and an alkaline earth metal to the reaction liquid obtained by the obtaining (2).
7. The method of claim 3 , wherein the (meth)acrylic acid anhydride remaining in a reaction liquid obtained by the obtaining (2) is hydrolyzed by addition of at least one basic compound selected from the group consisting of a hydroxide, a carbonate, a bicarbonate, and an oxide of at least one selected from the group consisting of an alkali metal and an alkaline earth metal to the reaction liquid obtained by the obtaining (2).
8. The method of claim 4 , wherein the (meth)acrylic acid anhydride remaining in a reaction liquid obtained by the obtaining (2) is hydrolyzed by addition of at least one basic compound selected from the group consisting of a hydroxide, a carbonate, a bicarbonate, and an oxide of at least one selected from the group consisting of an alkali metal and an alkaline earth metal to the reaction liquid obtained by the obtaining (2).
9. The method of claim 5 , wherein the (meth)acrylic acid anhydride is hydrolyzed by addition of 0.1 to 10 moles of water for 1 mole of the (meth)acrylic acid anhydride remaining in the reaction liquid obtained by the obtaining (2), to the reaction liquid.
10. The method of claim 6 , wherein the (meth)acrylic acid anhydride is hydrolyzed by addition of 0.1 to 10 moles of water for 1 mole of the (meth)acrylic acid anhydride remaining in the reaction liquid obtained by the obtaining (2), to the reaction liquid.
11. The method of claim 7 , wherein the (meth)acrylic acid anhydride is hydrolyzed by addition of 0.1 to 10 moles of water for 1 mole of the (meth)acrylic acid anhydride remaining in the reaction liquid obtained by the obtaining (2), to the reaction liquid.
12. The method of claim 8 , wherein the (meth)acrylic acid anhydride is hydrolyzed by addition of 0.1 to 10 moles of water for 1 mole of the (meth)acrylic acid anhydride remaining in the reaction liquid obtained by the obtaining (2), to the reaction liquid.
13. The method of claim 1 , wherein, in the fatty acid anhydride of formula (I), R 1 is a linear alkyl group.
14. The method of claim 1 , wherein, in the fatty acid anhydride of formula (I), R 1 is a branched alkyl group.
15. The method of claim 1 , wherein, in the fatty acid anhydride of formula (I), R 1 has a carbon number 1.
16. The method of claim 1 , wherein, in the fatty acid anhydride of formula (I), R 1 has a carbon number 2.
17. The method of claim 1 , wherein, in the fatty acid anhydride of formula (I), R 1 has a carbon number 3.
18. The method of claim 13 , wherein, in the fatty acid anhydride of formula (I), R 1 has a carbon number 3.