Method of producing an aminoalkylalkoxysilane
View Patent ↗A method of preparing an aminoalkylalkoxysilane, the method comprising reacting a haloalkylalkoxysilane with ammonia in a high pressure reactor for an amount of time sufficient to consume from 20 to 99.99% (w/w) of the haloalkylalkoxysilane and form an aminoalkylalkoxysilane; venting ammonia from the reactor to give a mixture comprising the aminoalkylalkoxysilane, unreacted haloalkylalkoxysilane, and an ammonium halide; and treating the mixture with a primary amine to form an N-substituted aminoalkylalkoxysilane.
1. A method of preparing an aminoalkylalkoxysilane, the method comprising:
(i) reacting a haloalkylalkoxysilane having the formula X(CH 2 ) m SiR 1 n (OR 1 ) 3-n (I) or
with ammonia in a high pressure reactor at a temperature from 30 to 200 ° C. and for an amount of time sufficient to consume from 20 to 99.99% (w/w) of the haloalkylalkoxysilane and form an aminoalkylalkoxysilane, wherein each R 1 is independently selected from C 1 -C 10 hydrocarbyl, each R 2 is independently selected from —H, and C 1 -C 4 hydrocarbyl, m is 1, 2, 3, 4, 5 or 6, n is 0, 1, or 2, p is 0 or 1, q is 2, 3, 4, or 5, and X is halo;
(ii) venting ammonia from the reactor to give a mixture comprising the aminoalkylalkoxysilane, unreacted haloalkylalkoxysilane, and an ammonium halide; and
(iii) treating the mixture with a primary amine having a boiling point of at least 115 ° C. such that the primary amine reacts with the unreacted haloalkylakoxysilane to form an N-substituted aminoalkylalkoxysilane.
2. The method of claim 1 wherein the haloalkylalkoxysilane has the formula X(CH 2 ) m SiR l n (OR 1 ) 3-n , wherein each R l is independently ethyl or methyl, m is 3, n is 0, and X is chloro.
3. The method of claim 1 , wherein the haloalkylalkoxysilane is reacted with the ammonia for an amount of time sufficient to consume from 70 to 99.98% (w/w) of the haloalkylalkoxysilane.
4. The method of claim 1 , wherein the haloalkylalkoxysilane and ammonia are reacted for from 0.5 hours to 2.5 hours.
5. The method of claim 1 , wherein the ammonia and the haloalkylalkoxysilane are reacted at a gauge pressure from 3400 to 5500 kPa.
6. The method of claim 1 , wherein the primary amine has a boiling point from 115 to 400 ° C.
7. The method of claim 1 , wherein the primary amine has the formula H 2 N(—R 3 NH—) c H, wherein each R 3 is independently hydrocarbylene and c is 1, 2, 3 or 4, or H 2 NR 4 , wherein R 4 is hydrocarbyl.
8. The method of claim 1 wherein the mixture is treated with the primary amine at a temperature from 50 to 150 ° C.
9. The method of claim 1 wherein the mixture is treated with the primary amine for from 5 minutes to 2.5 hours.
10. The method of claim 1 wherein the mixture is treated with from 0.5 to 40 moles of primary amine per mole of haloalkylalkoxysilane in the mixture.
11. The method of claim 1 , the method further comprising recovering the aminoalkylalkoxysilane and the N-substituted aminoalkylalkoxysilane.
12. The method of claim 1 , the method further comprising removing the ammonium halide.
13. The method of claim 1 , further comprising separating the aminoalkylalkoxysilane and the N-substituted aminoalkylalkoxysilane.
14. The method of claim 1 wherein the aminoalkylalkoxysilane has the formula H 2 N(CH 2 ) m SiR 1 n (OR 1 ) 3-n (III) or
wherein each R 1 is independently selected from C 1 -C 10 hydrocarbyl, each R 2 is independently selected from —H and C 1 -C 4 hydrocarbyl, m is 1, 2, 3, 4, 5 or 6, n is 0, 1 or 2, p is 0 or 1, and q is 2, 3, 4 or 5.
15. The method of claims 1 , wherein the N-substituted aminoalkylalkoxysilane has the formula YNH(CH 2 ) m SiR 1 n (OR 1 ) 3-n (V) or
wherein each R 1 is independently selected from C 1 -C 10 hydrocarbyl, each R 2 is independently selected from —H and C 1 -C 4 hydrocarbyl, m is 1, 2, 3, 4, 5, or 6, p is 0 or 1, q is 2, 3, 4, or 5 and Y is —R 3 NH(R 3 NH) c H or R 4 , wherein R 3 is hydrocarbylene, R 4 is hydrocarbyl, and c is 0, 1, 2, or 3.