IP Library Granted Patent US 12,152,004
Granted Patent B2
US 12,152,004 · App. 17/054,811 · Granted Nov 26, 2024

Systems and processes for producing organic acids directly from beta-lactones

Inventor: Sadesh H. Sookraj (Rochester, NY)
Assignee: Novomer, Inc.
C07C51/09B01J3/006B01J8/067C07C67/28C07C231/12C07C309/22C07D307/54C07D317/30C07F7/1804C07F7/1892B01J2219/0004
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Quick Facts
Patent No.
US 12,152,004
App. No.
17/054,811
Granted
Nov 26, 2024
Kind
B2
Abstract

Provided herein are reactor systems and processes for producing organic acids directly from beta-lactones. Such reactor systems and processes involve the use of a heterogeneous catalyst, such as a zeolite at vapor phase conditions. The reactor systems and processes may use a fixed bed, moving bed or fluidized contacting zone as reactor configurations.

Claims (38)

1. A process for producing an organic acid directly from a beta-lactone reagent, wherein the beta-lactone reagent is represented by the following formula:

wherein R 1 and R 2 are independently selected from the group consisting of H, alkyl, alkenyl, alkoxy, alkynyl, cycloalkyl, cycloalkenyl and cycloalkynyl, and

wherein both of R 1 and R 2 are not H at the same time,

the method comprising:

introducing the beta-lactone reagent to a reaction vessel;

contacting the beta-lactone reagent with a heterogenous catalyst in the reaction vessel to produce the organic acid; and

removing the organic acid from the reaction vessel, wherein the organic acid is an unsaturated aliphatic carboxylic acid that corresponds to the beta-lactone reagent.

2. The process of claim 1 , wherein the heterogenous catalyst comprises a zeolite.

3. The process of claim 2 , wherein the zeolite catalyst is in a hydrogen form or in metal cation exchanged form.

4. The process of claim 3 , wherein the metal cation is Na + , K + , Ca 2+ , Mg 2+ , Cu 2+ , or Cu + .

5. The process of claim 1 , wherein the organic acid is produced continuously.

6. The process of claim 1 , wherein the beta-lactone reagent is introduced to the reaction vessel combined with a solvent.

7. The process of claim 1 , wherein the reaction vessel further comprises a continuous fixed-bed reactor operating at a pressure between 250 Torr (4.834 psig) and 50 psig.

8. The process of claim 1 , wherein the reaction vessel further comprises a continuous fixed-bed reactor configured for receiving the beta-lactone reagent diluted with inert gas.

9. The process of claim 1 , wherein the least one reaction vessel further comprises a fluidized bed reactor configured to receive the beta-lactone reagent diluted with nitrogen.

10. The process of claim 1 , wherein the least one reaction vessel further comprises a tubular shell-and-tube reactor with a heterogenous catalyst loaded into the tubes and heat transfer fluid fed to the shell side to facilitate temperature control and removal of the heat produced during the reactions.

11. The process of claim 1 , wherein the organic acid is continuously isolated.

12. The process of claim 1 , wherein the organic acid is produced at a yield of at least 50%.

13. The process of claim 1 , wherein the organic acid is produced at a temperature between 100° C. and 300° C.

14. The process of claim 1 , wherein one of R 1 and R 2 is H, and the other of R 1 and R 2 is alkyl.

15. The process of claim 14 , wherein R 1 is alkyl, and R 2 is H.

16. A process for producing an organic acid directly from a beta-lactone reagent, wherein the beta-lactone reagent is a substituted beta-propiolactone represented by the following formula:

wherein R 1 and R 2 are independently selected from the group consisting of H, alkyl, alkenyl, alkoxy, alkynyl, cycloalkyl, cycloalkenyl and cycloalkynyl, and

wherein both of R 1 and R 2 are not H at the same time,

the method comprising:

introducing the beta-lactone reagent to a reaction vessel;

contacting the beta-lactone reagent with a heterogenous catalyst, wherein the heterogenous catalyst is a zeolite, in the reaction vessel to produce the organic acid; and

removing organic acid from the reaction vessel, wherein the organic acid is an unsaturated aliphatic carboxylic acid that corresponds to the substituted beta-propiolactone.

17. The process of claim 16 , wherein the zeolite catalyst is in a hydrogen form or in metal cation exchanged form.

18. The process of claim 16 , wherein the beta-lactone reagent is introduced to the reaction vessel combined with a solvent.

19. The process of claim 16 , wherein the reaction vessel further comprises a continuous fixed-bed reactor configured for receiving the beta-lactone reagent diluted with inert gas.

20. A process for producing an organic acid directly from a beta-lactone reagent, wherein the beta-lactone reagent is a substituted beta-propiolactone represented by the following formula:

wherein R 1 and R 2 are independently selected from the group consisting of H, alkyl, alkenyl, alkoxy, alkynyl, cycloalkyl, cycloalkenyl and cycloalkynyl, and

wherein both of R 1 and R 2 are not H at the same time and one of R 1 and R 2 is H,

the method comprising:

introducing the beta-lactone reagent to a reaction vessel;

contacting the beta-lactone reagent with a heterogenous catalyst, wherein the heterogenous catalyst is a zeolite, in the reaction vessel to produce the organic acid; and

removing organic acid from the reaction vessel, wherein the organic acid is an unsaturated aliphatic carboxylic acid that corresponds to the substituted beta-propiolactone.

Assignments (4)
CHANGE OF NAME Recorded Mar 24, 2026
From: NMER WINDDOWN, INC.
To: NOVOMER LLC
Reel/Frame 075187/0876 →
RELEASE OF SECURITY INTEREST Recorded Aug 5, 2022
From: TRUIST BANK
To: NOVOMER, INC.
Reel/Frame 061088/0116 →
SECURITY INTEREST Recorded Feb 1, 2022
From: NOVOMER, INC.
To: TRUIST BANK
Reel/Frame 058922/0803 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 14, 2020
From: SOOKRAJ, SADESH H.
To: NOVOMER, INC.
Reel/Frame 054415/0089 →
Continuity (5)
Continuation 16023410 · Jun 29, 2018
Continuation In Part 15640197 · Jun 30, 2017
Continuation In Part 15464346 · Mar 21, 2017
Provisional Application 62311262 · Mar 21, 2016
Related Publication 20210221762A1 · Jul 22, 2021