IP Library Granted Patent US 10,870,724
Granted Patent B2
US 10,870,724 · App. 16/571,267 · Granted Dec 22, 2020

High heat monomers and methods of use thereof

Inventors: Edward Norman Peters (Lenox, MA); Scott Michael Fisher (Delmar, NY); Jaykisor Pal (Bangalore, IN)
Assignee: SABIC GLOBAL TECHNOLOGIES B.V.
C08G59/063C07D303/18C07D303/27C07D405/12C07D405/14C08G59/245C09D163/00
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Quick Facts
Patent No.
US 10,870,724
App. No.
16/571,267
Granted
Dec 22, 2020
Kind
B2
Abstract

High purity epoxide compounds methods for preparing the high purity epoxide compounds, and compositions derived from the epoxide compounds are provided. Also provided are materials and articles derived from the epoxide compounds.

Claims (21)

1. A compound having formula:

wherein R 1 and R 2 at each occurrence are each independently selected from an epoxide-containing functional group; R a and R b at each occurrence are each independently halogen, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 3 -C 8 cycloalkyl, or C 1 -C 12 alkoxy; p and q at each occurrence are each independently 0 to 4; R 13 at each occurrence is independently a halogen or a C 1 -C 6 alkyl group; c at each occurrence is independently 0 to 4; R 14 at each occurrence is independently a C 1 -C 6 alkyl, phenyl, or phenyl substituted with up to five halogens or C 1 -C 6 alkyl groups; R g at each occurrence is independently C 1 -C 12 alkyl or halogen, or two R g groups together with the carbon atoms to which they are attached form a four-, five, or six-membered cycloalkyl group; and t is 0 to 10;

wherein the compound has a purity of 97% or greater, as determined by high performance liquid chromatography (HPLC);

the compound has an oligomer impurity content of less than or equal to 1%, as determined by high performance liquid chromatograph, and

the compound has a softening point of less than 50° C., as measured according to ASTM E28-1999.

2. The compound of claim 1 , wherein R 1 and R 2 at each occurrence are each selected from:

wherein R 3a and R 3b are each independently selected hydrogen and C 1 -C 12 alkyl.

3. The compound of claim 1 , wherein the compound is substantially free of oligomer impurities.

4. The compound of claim 1 , having formula (1-a), (2-a), or (4-b)

5. The compound of claim 4 , wherein the compound has an oligomer impurity content of less than or equal to 0.5%, as determined by high performance liquid chromatography.

6. The compound of claim 4 , wherein the compound has an oligomer impurity content of less than or equal to 0.1%, as determined by high performance liquid chromatography.

7. The compound of claim 4 , wherein the compound has formula (1-a).

8. The compound of claim 4 , wherein the compound has formula (2-a).

9. The compound of claim 4 , wherein the compound has formula (4-b).

10. The compound of claim 1 , wherein the compound has a metal impurity content of 1 ppm or less.

11. The compound of claim 1 , wherein the compound has a color APHA value of 20 or less, as measured using test method ASTM D1209.

12. The compound of claim 1 , having formula (4-c):

13. The compound of claim 1 , having formula (6-a):

14. The compound of claim 1 , having formula (7-a):

15. The compound of claim 1 , having formula (8-a):

16. The compound of claim 1 , having formula (9-a):

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE REMOVE THE APPLICATION NUMBER 15039474 PREVIOUSLY RECORDED AT REEL: 054528 FRAME: 0467. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 23, 2021
From: SABIC GLOBAL TECHNOLOGIES B.V.
To: SHPP GLOBAL TECHNOLOGIES B.V.
Reel/Frame 057453/0680 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2020
From: SABIC GLOBAL TECHNOLOGIES B.V.
To: SHPP GLOBAL TECHNOLOGIES B.V.
Reel/Frame 054528/0467 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2019
From: PETERS, EDWARD NORMAN; FISHER, SCOTT MICHAEL; PAL, JAYKISOR
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 050379/0547 →
Continuity (3)
Continuation 15327416
Provisional Application 62027600 · Jul 22, 2014
Related Publication 20200010608A1 · Jan 9, 2020