IP Library Granted Patent US 7,923,572
Granted Patent B2
US 7,923,572 · App. 12/067,746 · Granted Apr 12, 2011

Method for producing ketimine structure-containing alkoxysilane

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Quick Facts
Patent No.
US 7,923,572
App. No.
12/067,746
Granted
Apr 12, 2011
Kind
B2
Abstract

A method for producing ketimine structure-containing alkoxysilane comprising reacting amino-functional alkoxysilane with a monocarbonyl compound by heating and azeotropically distilling off the produced water together with the monocarbonyl compound to yield ketimine structure-containing alkoxysilane, characterized by introducing additional monocarbonyl compound at the time of the azeotropic distillation of the produced water together with the monocarbonyl compound.

Claims (13)

1. A method for producing ketimine structure-containing alkoxysilane comprising;

reacting an amino-functional alkoxysilane represented by general formula (1)

(wherein R 1 represents C 1-6 monovalent hydrocarbyl, R 2 represents C 1-4 alkyl, R 3 represents C 1-10 divalent hydrocarbyl or a divalent organic group represented by —R 4 —NH—R 5 — (wherein R 4 and R 5 represent C 1-10 divalent hydrocarbyl), and n is 1, 2, or 3) with a monocarbonyl compound represented by general formula (2)

(wherein R 6 and R 7 represent the hydrogen atom or C 1-10 monovalent hydrocarbyl, but do not simultaneously represent the hydrogen atom) by heating and azeotropically distilling off the produced water along with the monocarbonyl compound to yield ketimine structure-containing alkoxysilane represented by general formula (3)

(wherein R 1 , R 2 , R 3 , R 6 , R 7 , and n are defined as above),

characterized by introducing additional monocarbonyl compound at the time of the azeotropic distillation of the produced water along with the monocarbonyl compound of formula (2).

2. The method according to claim 1 for producing ketimine structure-containing alkoxysilane, wherein the amount of monocarbonyl compound that is additionally introduced at the time of the azeotropic distillation of the produced water along with the monocarbonyl compound is from 1 to 10 moles per 1 mole of the amino-functional alkoxysilane.

3. The method according to claim 1 for producing ketimine structure-containing alkoxysilane, characterized in that the temperature of the reaction between the monocarbonyl compound and the amino-functional alkoxysilane is at least the temperature of the water/monocarbonyl compound azeotrope and is in a range that does not exceed the boiling point of the monocarbonyl compound.

4. The method according to claim 1 for producing ketimine structure-containing alkoxysilane, characterized in that the amino-functional alkoxysilane is selected from the group consisting of (CH 3 O) 3 Si(CH 2 ) 3 NH 2 , (CH 3 CH 2 O) 3 Si(CH 2 ) 3 NH 2 , (CH 3 O) 3 Si(CH 2 ) 3 NH(CH 2 ) 2 NH 2 , and (CH 3 CH 2 O) 3 Si(CH 2 ) 3 NH(CH 2 ) 2 NH 2 .

5. The method according claim 1 for producing ketimine structure-containing alkoxysilane, characterized in that the monocarbonyl compound is methyl isobutyl ketone.

6. The method according to claim 2 for producing ketimine structure-containing alkoxysilane, characterized in that the monocarbonyl compound is methyl isobutyl ketone.

7. The method according to claim 3 for producing ketimine structure-containing alkoxysilane, characterized in that the monocarbonyl compound is methyl isobutyl ketone.

8. The method according to claim 4 for producing ketimine structure-containing alkoxysilane, characterized in that the monocarbonyl compound is methyl isobutyl ketone.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2019
From: DOW CORNING TORAY CO., LTD.
To: DOW TORAY CO., LTD.
Reel/Frame 051322/0925 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2009
From: TANIGUCHI, YOSHINORI; IWAI, MAKOTO; WAKITA, KEIJI
To: DOW CORNING TORAY COMPANY, LTD.
Reel/Frame 022273/0555 →