IP Library Granted Patent US 7,005,281
Granted Patent B2
US 7,005,281 · App. 10/506,698 · Granted Feb 28, 2006

Enzymatic process for preparing organosilicon group containing photoinitiators

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Quick Facts
Patent No.
US 7,005,281
App. No.
10/506,698
Granted
Feb 28, 2006
Kind
B2
Abstract

The invention relates to a process for preparing organosilicon group containing photoinitiators of the formula (I), wherein m is a number from 1 to 200; q is 0 or 1; A is IN-C(O)—O—CHR 3 —Y— or IN-C(O)—NH—CHR 3 —Y—; A′ is A or R 1 ′; R 1 and R 1 ′, R 2 and R 2 ′ are C 1 –C 18 alkyl or phenyl, or —(O) q —SiR 1 R 1 ′R 2 ; R 3 is hydrogen or C 1 –C 6 alkyl, Y is a divalent group selected from C 1 –C 10 alkeylene, C 2 –C 10 alkenylene or —(CH 2 ) b —O—(CH 2 ) a —; and b are each independently of the other a number of 1 to 6; IN is a photolabile functional moiety of the formula (II) or (III), wherein R 4 is hydrogen or —C(O)—C(O)—OH or —C(O)—C(O)—OC 1 –C 6 alkyl and n is 1–3; R 5 and R 6 are C 1 –C 12 alkyl or together are cycloC 5 –C 7 alkyl; R 7 is hydroxy, C 1 –C 6 alkoxy or morpholinyl; X is —(CH 2 ) a —, —(CH 2 ) b —O—(CH 2 ) a — or —(CH 2 ) b —O—CO—(CH 2 ) a —; a and b are each independently of the other a number of 1 to 6; whereby the process is characterized in that a photolabile functional moiety containing a carboxy group (IN-COOH) or an alkoxycarbonyl group (IN-CO—OC 1 –C 6 alkyl) is reacted with a carbinol- or amino terminated organosilicon compound of the formula (IV), wherein m, R 1 and R 1 ′, R 2 and R 2 ′ are as defined above and B is —Y—CHR 3 —OH or —Y—CHR 3 —NH 2 ; B′ is B or R 1 ′, in the presence of an enzyme which catalyzes the esterification, transesterification or amidation reaction.

Claims (57)

1. A process for preparing organosilicon group containing photoinitiators of the formula I

wherein

m is a number from 1 to 200;

q is 0 or 1;

A is IN-C(O)—O—CHR 3 —Y— or IN-C(O)—NH—CHR 3 —Y—;

A′ is A or R 1 ′;

R 1 and R 1 ′, R 2 and R 2 ′ independently of one another are C 1 –C 18 alkyl or phenyl or —(O) q —SiR, R 1 ′R 2 ;

R 3 is hydrogen or C 1 –C 6 alkyl,

Y is a divalent group C 1 –C 10 alkylene, C 2 –C 10 alkenylene or —(CH 2 ) b —O—(CH 2 ) a —; a and b are each independently of the other a number of 1 to 6;

IN is a photolabile functional moiety of the formula II or III

 wherein

R 4 is hydrogen or —C(O)—C(O)—OH or —C(O)—C(O)—OC 1 –C 6 alkyl and n is 1–3;

R 5 and R 6 are C 1 –C 12 alkyl or together are cycloC 5 –C 7 alkyl;

R 7 is hydroxy, C 1 –C 6 alkoxy or morpholinyl;

X is —(CH 2 ) a —, —(CH 2 ) b —O—(CH 2 ) a — or —(CH 2 ) b —O—CO—(CH 2 ) a —; a and b are each independently of the other a number of 1 to 6;

which process comprises

reacting a photolabile functional moiety containing a carboxy group (IN-COOH) or an alkoxycarbonyl group (IN-CO—OC 1 –C 6 alkyl) with a carbinol or amino terminated organosilicon compound of the formula IV

 wherein m, R 1 and R 1 ′, R 2 and R 2 ′ are as defined above and

B is —Y—CHR 3 —OH or —Y—CHR 3 —NH 2 ;

B′ is B or R 1 ′,

in the presence of an enzyme which catalyzes the esterification, transesterification or amidation reaction.

2. A process according to claim 1 , wherein

m is a number from 1 to 20;

q is 0 or 1;

A is a group

A′ is A or R 1 ′;

R 1 and R 1 ′, R 2 and R 2 ′ independently of one another are methyl, —O—Si(CH 3 ) 3 or —Si(CH 3 ) 3 ;

Y is a divalent group C 1 –C 10 alkylene, C 2 –C 10 alkenylene or —(CH 2 ) b —O—(CH 2 ) a —; a and b are each independently of the other a number of 1 to 6;

which process comprises

reacting a photolabile functional moiety containing a carboxy group (IN-COOH) or an alkoxycarbonyl group (IN-CO—OC 1 –C 6 alkyl) with a carbinol or amino terminated organosilicon compound of the formula IV

 wherein m, R 1 and R 1 ′, R 2 and R 2 ′ are as defined above and

B is —Y—CH 2 —OH or —Y—CH 2 —NH 2 ;

B′ is B or R 1 ′,

in the presence of an enzyme selected from the group consisting of esterases, lipases and proteases.

3. A process according to claim 1 , wherein

m is a number from 1 to 20;

q is 0 or 1;

A is a group of the formula IIIa or IIIb

A′ is A or R 1 ′;

R 1 and R 1 ′, R 2 and R 2 ′ independently of one another are methyl, —O—Si(CH 3 ) 3 or —Si(CH 3 ) 3 ;

Y is a divalent group C 1 –C 10 alkylene, C 2 –C 10 alkenylene or —(CH 2 ) b —O—(CH 2 ) a —; a and b are each independently of the other a number of 1 to 6;

X is —(CH 2 ) a —, —(CH 2 ) b —O—(CH 2 ) a — or —(CH 2 ) b —O—CO—(CH 2 ) a —; a and b are each independently of the other a number of 1 to 6;

which process comprises

reacting a photolabile functional moiety containing a carboxy group (IN-COOH) or an alkoxycarbonyl group (IN-CO—OC 1 –C 6 alkyl) with a carbinol or amino terminated organosilicon compound of the formula IV

 wherein m, R 1 and R 1 ′, R 2 and R 2 ′ are as defined above and

B is —Y—CH 2 —OH or —Y—CH 2 —NH 2 ;

B′ is B or R 1 ′,

in the presence of an enzyme selected from the group consisting of esterases, lipases and proteases.

4. A process according to claim 1 , wherein the enzyme is immobilized on a support.

5. A process according to claim 1 , wherein the reaction is carried out at a temperature in the range from 25° C. to 75° C.

6. A process according to claim 2 , wherein the enzyme is immobilized on a support.

7. A process according to claim 3 , wherein the enzyme is immobilized on a support.

8. A process according to claim 2 , wherein the reaction is carried out at a temperature in the range from 25° C. to 75° C.

9. A process according to claim 3 , wherein the reaction is carried out at a temperature in the range from 25° C. to 75° C.

10. A process according to claim 4 , wherein the reaction is carried out at a temperature in the range from 25° C. to 75° C.

11. A process according to claim 6 , wherein the reaction is carried out at a temperature in the range from 25° C. to 75° C.

12. A process according to claim 7 , wherein the reaction is carried out at a temperature in the range from 25° C. to 75° C.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2020
From: BASF SE
To: IGM GROUP B.V.
Reel/Frame 052450/0001 →
CHANGE OF NAME Recorded Apr 20, 2020
From: CIBA SPECIALTY CHEMICALS CORPORATION
To: CIBA CORPORATION
Reel/Frame 052444/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2020
From: CIBA CORPORATION
To: BASF SE
Reel/Frame 052446/0891 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2005
From: OHRLEIN, REINHOLD; SCHONING, KAI-UWE; BAISCH, GABRIELE; SCHMIDT, JEMIMA; BAUDIN, GISELE; JUNG, TUNJA
To: CIBA SPECIALTY CHEMICALS CORP.
Reel/Frame 017070/0153 →