Process for preparing aspartates
View Patent ↗The present invention relates to novel aspartates, their method of production and the use of these mono and polyaspartates as reactive components for polyisocyanates in two-component polyurethane coating compositions and for preparing polyurethane prepolymers.
1. An aspartate of the formula:
where
X represents an m-valent organic residue obtained by removing the primary amino group or groups from a mono or polyamine which has (cyclo)aliphatically bound amino groups and a number average molecular weight of 60 to 6000, and which may contain further functional groups that either are reactive with isocyanate groups or are inert to isocyanate groups at temperatures of up to 100° C.,
R 1 and R 2 may be identical or different and represent hydrogen or organic groups which are inert towards isocyanate groups at a temperature of 100° C. or less,
R 3 and R 4 may be identical or different and represent organic groups which are inert towards isocyanate groups at a temperature of 100° C. or less,
R 5 represents hydrogen or together with R 5′ and the carbon atoms to which they are connected forms a six-membered cycloalkyl group, with said cycloalkyl group being substituted with from 0 to 3 alkyl groups having from 1 to 3 carbon atoms,
R 5′ represents a moiety selected from the group consisting of i) C 1 to C 8 alkyl groups which may be interrupted with an oxygen atom, ii) C 6 to C 10 aryl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms and iii) C 6 to C 12 cycloalkyl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms,
R 6 represents hydrogen or together with R 6′ and the carbon atoms to which they are connected forms a six-membered cycloalkyl group, with said cycloalkyl group being substituted with from 0 to 3 alkyl groups having from 1 to 3 carbon atoms,
R 6′ represents a moiety selected from the group consisting of i) C 1 to C 8 alkyl groups which may be interrupted with an oxygen atom, ii) C 6 to C 10 aryl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms and iii) C 6 to C 12 cycloalkyl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms,
with the proviso that R 5 and R 6 are the same and R 5′ and R 6′ are the same, and
a and b represent integers of from 1 to 5, provided that the sum of a and b is from 2 to 6.
2. A process for preparing an asparatate of the formula:
where
X represents an m-valent organic residue obtained by removing the primary amino group or groups from a mono or polyamine which has (cyclo)aliphatically bound amino groups and a number average molecular weight of 60 to 6000, and which may contain further functional groups that either are reactive with isocyanate groups or are inert to isocyanate groups at temperatures of up to 100° C.,
R 1 and R 2 may be identical or different and represent hydrogen or organic groups which are inert towards isocyanate groups at a temperature of 100° C. or less,
R 3 and R 4 may be identical or different and represent organic groups which are inert towards isocyanate groups at a temperature of 100° C. or less,
R 5 represents hydrogen or together with R 5′ and the carbon atoms to which they are connected forms a six-membered cycloalkyl group, with said cycloalkyl group being substituted with from 0 to 3 alkyl groups having from 1 to 3 carbon atoms,
R 5′ represents a moiety selected from the group consisting of i) C 1 to C 8 alkyl groups which may be interrupted with an oxygen atom, ii) C 6 to C 10 aryl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms and iii) C 6 to C 12 cycloalkyl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms,
R 6 represents hydrogen or together with R 6′ and the carbon atoms to which they are connected forms a six-membered cycloalkyl group, with said cycloalkyl group being substituted with from 0 to 3 alkyl groups having from 1 to 3 carbon atoms,
R 6′ represents a moiety selected from the group consisting of i) C 1 to C 8 alkyl groups which may be interrupted with an oxygen atom, ii) C 6 to C 10 aryl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms and iii) C 6 to C 12 cycloalkyl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms,
with the proviso that R 5 and R 6 are the same and R 5′ and R 6′ are the same, and
a and b represent integers of from 1 to 5, provided that the sum of a and b is from 2 to 6, comprising
A) reacting at a temperature of 0 to 100° C., in solution or in the absence of a solvent and at an equivalent ratio of primary amino groups in component a) to C═C double bonds in component b) of from about 1.1:1 to about 3.0:1
a) mono or polyamines corresponding to formula (II)
X[—NH 2 ] m (II)
with
b) compounds corresponding to formula (III)
R 3 OOC—C(R 1 )═C(R 2 )—COOR 4 (III)
wherein
X, R 1 , R 2 , R 3 and R 4 are as defined above and
m represents an integer of from 2 to 6, and
B) reacting the resultant product with an oxirane compound selected from the group consisting of alkylene oxides, cycloalkylene oxides, and phenyl glycidyl ether.
3. A two-component coating composition which comprises, as binder,
a) a polyisocyanate component and
b) an isocyanate-reactive component containing
b1) the aaspartate of claim 1 ,
b2) optionally other isocyanate-reactive compounds,
wherein the equivalent ratio of isocyanate groups to isocyanate-reactive groups is from about 0.8:1 to about 2.0:1.
4. A prepolymer containing urea, urethane, allophanate and/or biuret structures comprising the reaction product of a polyisocyanate with the aspartate of claim 1 .