IP Library Granted Patent US 10,967,364
Granted Patent B2
US 10,967,364 · App. 15/561,212 · Granted Apr 6, 2021

Catalysts and methods for forming alkenyl and alkyl substituted arenes

Inventors: Thomas B. Gunnoe (Palmyra, VA); Benjamin Austin Vaughan (Dover, NH); Michael S. Webster-Gardiner (Mims, FL)
Assignee: University of Virginia Patent Foundation
B01J31/1815B01J31/00B01J31/189B01J31/2226B01J31/2291C07C2/66C07C5/03B01J2231/46B01J2531/0244B01J2531/822B01J2540/22B01J2540/225
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Quick Facts
Patent No.
US 10,967,364
App. No.
15/561,212
Granted
Apr 6, 2021
Kind
B2
Abstract

Embodiments of the present disclosure provide for Rh(I) catalysts, methods of making alkenyl substituted arenes (e.g., allyl arene, vinyl arene, and the like), methods of making alkyl substituted arenes, and the like.

Claims (19)

1. A method of making a substituted arene, comprising reacting an arene and olefin with a catalyst and an oxidant, with the proviso that the method is performed in the absence of CO, wherein the catalyst is:

wherein A 1 and A 2 are independently selected from the group consisting of a halogen and an acetate group; and R 21 , R 22 , R 23 , and R 24 are each independently selected from an olefin:

wherein the oxidant is a copper(II) salt, iodate, periodate, nitrogen dioxide, silver salt, peroxide, dioxygen, air, or a combination thereof;

wherein the arene is benzene or naphthalene, wherein the arene is optionally substituted with 1-4 substituents selected from the group consisting of halo, methyl, carboxylate, nitro, and alkoxy;

wherein the olefin is:

and

R is hydrogen, a halide, an alkyl, an alkenyl, a carbocycle group, a heterocyclo, an aryl, or a heteroaryl;

to form a product, wherein the product is

2. The method of claim 1 , wherein the reacting is at a reaction temperature of 100° C. to 300° C.

3. The method of claim 2 , wherein the reaction temperature is 100° C. to 250° C.

4. The method of claim 1 , further comprising:

reacting the product with a second catalyst in the presence of H 2 , wherein the second catalyst is selected from the group consisting of: Pt/C, Pd/C, Raney Ni, Wilkinson's Catalyst, and PtO 2 .

5. The method of claim 1 , wherein the arene is selected from the group consisting of benzene, naphthalene, toluene, xylene, mesitylene, chlorobenzene, fluorobenzene, bromobenzene, iodobenzene, dichlorobenzene, difluorobenzene, or dibromobenzene.

6. The method of claim 1 , wherein the arene is benzene, naphthalene, or toluene.

7. The method of claim 1 , wherein the olefin is ethylene, propylene, pentene, hexene, or isobutylene.

8. The method of claim 1 , wherein the arene and olefin are present in a molar ratio of arene to olefin of 1:100 to 1000:1.

9. The method of claim 1 , wherein the catalyst is present in an amount of 5 mol % to 0.00001 mol % relative to arene.

10. The method of claim 1 , wherein the olefin is a gaseous olefin at a pressure of 10 psig to 5000 psig.

11. The method of claim 1 , wherein the olefin is a gaseous olefin at a pressure of 10 psig to 90 psig.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2021
From: GUNNOE, THOMAS B.; VAUGHAN, BENJAMIN AUSTIN; WEBSTER-GARDINER, MICHAEL S.
To: UNIVERSITY OF VIRGINIA
Reel/Frame 055403/0576 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2021
From: UNIVERSITY OF VIRGINIA
To: UNIVERSITY OF VIRGINIA PATENT FOUNDATION
Reel/Frame 055415/0029 →
CONFIRMATORY LICENSE Recorded Jan 17, 2020
From: UNIVERSITY OF VIRGINIA
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 051639/0545 →
Continuity (2)
Provisional Application 62137853 · Mar 25, 2015
Related Publication 20180065116A1 · Mar 8, 2018
Cited By (1)
US 12,404,221