Method of preparing quaternary ammonium hydroxide and quaternary ammonium carbonate in an aminoalcohol solvent
View Patent ↗This invention provides a method of preparing a quaternary ammonium hydroxide compound having the formula (NR 1 R 2 R 3 R 4 )OH, wherein R 1 and R 2 are independently C 1 –C 4 alkyl; R 3 is benzyl or a C 1 –C 20 alkyl or a C 1 –C 20 aryl-sutstituted alkyl; R 4 is a C 8 –C 20 alkyl. The method includes the step of reacting a quaternary ammonium compound having the formula (NR 1 R 2 R 3 R 4 ) + X − , wherein R 1 , R 2 , R 3 , and R 4 are as defined above and X is Br or Cl, with a metal hydroxide in an aminoalcohol solvent to yield the quaternary ammonium hydroxide. The reaction forms metal bromide and/or metal chloride as a byproduct. The metal byproducts and excess metal hydroxide (if any) can be removed by methods known in the art. According to one preferred embodiment, the reaction of the quaternary ammonium compound with the metal hydroxide is performed in an anhydrous environment (i.e., with no water present).
1. A method of preparing a quaternary ammonium hydroxide compound having the formula (NR 1 R 2 R 3 R 4 )OH, wherein
R 1 and R 2 are independently C 1 –C 4 alkyl;
R 3 is benzyl or a C 1 –C 20 alkyl or a C 1 –C 20 aryl-sutstituted alkyl;
R 4 is a C 8 –C 20 alkyl,
the method comprising the step of reacting a quaternary ammonium compound having the formula (NR 1 R 2 R 3 R 4 ) + X − , wherein R 1 , R 2 , R 3 , and R 4 are as defined above and X is Br or Cl, with a metal hydroxide in an aminoalcohol solvent to yield the quaternary ammonium hydroxide.
2. The method of claim 1 , further comprising the step of removing any metal chloride or metal bromide formed by the reaction of the quaternary ammonium compound and the metal hydroxide.
3. The method of claim 1 , where he reaction is performed in the absence of water.
4. The method of claim 1 , herein any excess metal hydroxide is removed after the reaction.
5. The method of claim 1 , wherein X is Cl.
6. The method of claim 1 , wherein X is Br.
7. The method of claim 1 , wherein R 3 is benzyl or a C 1 –C 20 alkyl.
8. The method of claim 1 , wherein R 1 and R 2 are methyl, and R 3 is benzyl.
9. The method of claim 5 , wherein R 4 is a C 8 –C 12 alkyl.
10. The method of claim 1 , wherein R 1 and R 2 are methyl and R 3 and R 4 are C 8 –C 12 alkyl.
11. The method of claim 1 , wherein R 3 and R 4 are decyl.
12. The method of claim 1 , wherein the aminoalcohol has the formula
wherein R 5 is hydrogen or a C 1 –C 3 alkyl; R 6 is a bond or a C 1 –C 3 alkyl.
13. The method of claim 12 , wherein R 5 is hydrogen or a linear C 1 –C 3 alkyl and R 6 is a linear C 1 –C 3 alkyl.
14. The method of claim 12 , wherein the aminoalcohol has the formula NH 2 —(CH 2 ) n —OH, wherein n is an integer from 2 to 6.
15. The method of claim 12 , wherein the aminoalcohol is ethanolamine.
16. A method of preparing a quaternary ammonium carbonate having the formula (NR 1 R 2 R 3 R 4 ) 2 CO 3 , wherein
R 1 and R 2 are independently C 1 –C 4 alkyl;
R 3 is a C 1 –C 20 alkyl or a C 1 –C 20 aryl-substituted alkyl;
R 4 is a C 8 –C 20 alkyl,
the method comprising the steps of:
(a) reacting a quaternary ammonium compound having the formula (NR 1 R 2 R 3 R 4 ) + X − , wherein R 1 , R 2 , R 3 , and R 4 are as defined above and X is Br or Cl, with a metal hydroxide in an aminoalcohol solvent to yield a quaternary ammonium hydroxide having the formula (NR 1 R 2 R 3 R 4 )OH; and
(b) reacting the quaternary ammonium hydroxide with a carbonate or bicarbonate source to yield the quaternary ammonium carbonate.