IP Library Granted Patent US 10,138,183
Granted Patent B2
US 10,138,183 · App. 15/137,900 · Granted Nov 27, 2018

Process and composition for inhibiting the polymerization of cyclopentadiene compounds

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,138,183
App. No.
15/137,900
Granted
Nov 27, 2018
Kind
B2
Abstract

A process for inhibiting the polymerization of cyclopentadiene compounds (B) by contacting the cyclopentadiene compound with a quinone methide compound (A) of structure (I), Compositions (AB) comprising (A) and (B) are also provided.

Claims (20)

1. A composition (AB), comprising:

a cyclopentadiene compound (B), and

a compound (A) of structure (I):

wherein

R 1 and R 2 are each tert-butyl; and

R 3 is —CN, —O—R 10 , or —R 12 , where R 10 is methyl, ethyl, n-propyl, iso-propyl, n-butyl, n-pentyl, or n-hexyl and R 12 is 2-furyl, 3-furyl, or phenyl.

2. The composition (AB) according to claim 1 , wherein the cyclopentadiene compound (B) is at least one selected from the group consisting of cyclopentadiene, dicyclopentadiene, alkylated cyclopentadiene and alkylated dicyclopentadiene.

3. The composition (AB) according to claim 1 , wherein the cyclopentadiene compound (B) is at least one of cyclopentadiene and dicyclopentadiene.

4. The composition (AB) according to claim 1 , wherein a concentration of the compound (A) of structure (I) is between 10 ppb (m/m) and 100,000 ppm (m/m), based on a total weight of the cyclopentadiene compound (B).

5. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —O—R 10 , where R 10 is methyl.

6. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —O—R 10 , where R 10 is ethyl.

7. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —O—R 10 , where R 10 is n-propyl.

8. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —O—R 10 , where R 10 is iso-propyl.

9. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —O—R 10 , where R 10 is n-butyl.

10. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —O—R 10 , where R 10 is n-pentyl.

11. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —O—R 10 , where R 10 is n-hexyl.

12. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —R 12 , where R 12 is 2-furyl.

13. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —R 12 , where R 12 is 3-furyl.

14. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —R 12 , where R 12 is phenyl.

15. The composition (AB) according to claim 1 , wherein, in the structure (I), R 3 is —CN.

Assignments (1)
CHANGE OF NAME Recorded Jan 31, 2020
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051765/0166 →