IP Library Granted Patent US 10,266,486
Granted Patent B2
US 10,266,486 · App. 16/070,326 · Granted Apr 23, 2019

Method of making a composition of an alkanolamine alkylamide and a polyol

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Quick Facts
Patent No.
US 10,266,486
App. No.
16/070,326
Granted
Apr 23, 2019
Kind
B2
Abstract

The disclosure generally provides methods for preparing compositions comprising alkanolamine alkylamides and polyols. This disclosure further relates to methods for preparing compositions comprising alkanolamine alkylamides and polyols that can be used in formulations that provide moisturization.

Claims (25)

1. A method of making a composition comprising a compound of formula (I)

wherein

Z is (a) a linear or branched C 2 -C 6 alkylene optionally substituted with one or more —OH or —(C 1 -C 3 alkyl)-OH, or (b) (—R 2 —O—R 3 —) n , where n is an integer from 1 to 5, and each R 2 and R 3 is independently —CH 2 —CR 4 H—, wherein R 4 is H or an unsubstituted linear or branched C 1 -C 3 alkyl; and

R 1 is an unsubstituted linear or branched C 1 -C 3 alkyl;

and a polyol,

the method comprising reacting an alkanolamine of formula (II)

with a polyol ester comprising at least one —C(O)R 1 moiety.

2. The method of claim 1 , wherein the polyol is derived by the cleavage of at least one —C(O)R 1 moiety from said polyol ester.

3. The method of claim 1 , wherein the polyol ester is of formula (III):

wherein

R 1 is an unsubstituted linear or branched C 1 -C 3 alkyl;

R 5 is a linear or branched C 3 -C 6 alkyl or a mono-, di-, oligo or poly-saccharide sugar group;

m is an integer from 1 to 10; and

p is an integer from 0 to 9, provided that sum of m and p is at least 2 and less than or equal to the number of carbon atoms in R 5 .

4. The method on claim 1 , wherein the reaction is conducted without a catalyst.

5. The method of claim 1 , wherein the reaction is conducted in the presence of a catalyst.

6. The method of claim 5 , wherein the catalyst is sodium carbonate, potassium carbonate, sulfuric acid, or phosphorous acid.

7. The method of claim 1 , wherein the reaction is conducted without additional solvent.

8. The method of claim 1 , wherein the reaction is conducted at a temperature of 100° C. to 140° C., or at 115° C. to 130° C., or at 120° C. to 125° C.

9. The method of claim 1 , wherein the molar ratio of the alkanolamine of formula (II) and the polyol ester is about X:1, or about X:1.01, or about X:1.05, or about X:1.1, or about X:1.15, or about X:1.2, or about X:1.25, wherein X is the number of —C(O)R 1 moieties on the polyol ester.

10. The method of claim 1 , wherein R 1 is selected from methyl and ethyl.

11. The method of claim 1 , wherein Z is a linear or branched C 2 -C 6 alkylene optionally substituted with one or more —OH or —(C 1 -C 3 alkyl)-OH.

12. The method of claim 1 , wherein Z is (—R 2 —O—R 3 —) n , where n is an integer from 1 to 4, and each R 2 and R 3 are independently selected from —CH 2 —CR 4 H—, and R 4 is H or an unsubstituted linear or branched C 1 -C 3 alkyl.

13. The method of claim 1 , wherein the polyol ester is 1,2,3-triacetoxypropane and the polyol is glycerol.

14. The method of claim 1 , wherein the compound of formula (I) is:

Assignments (3)
CHANGE OF NAME Recorded Sep 18, 2019
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 050426/0671 →
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 16, 2018
From: BEVINAKATTI, HANAMANTHSA; WHITE, KAREN LEE
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 046360/0200 →