IP Library Granted Patent US 7,045,654
Granted Patent B2
US 7,045,654 · App. 10/691,390 · Granted May 16, 2006

Method for the alkylation of salicylic acid

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Quick Facts
Patent No.
US 7,045,654
App. No.
10/691,390
Granted
May 16, 2006
Kind
B2
Abstract

A process is disclosed for the production of alkyl salicylic acids wherein the process comprises reacting salicylic acid with an olefin having at least four carbon atoms at elevated temperature in the presence of a perfluoroalkylsulfonic acid, an alkylsulfonic acid, or an acidic clay as a catalyst.

Claims (9)

1. A process for the production of alkyl salicylic acids comprising reacting salicylic acid with an olefin having at least four carbon atoms at an elevated temperature in the range of from about 50° C. to about 200° C. in the presence of a perfluoroalkylsulfonic acid, an alkylsulfonic acid, or an acidic clay as a catalyst.

2. The process of claim 1 wherein the catalyst is anhydrous methanesulfonic acid.

3. The process of claim 1 wherein the olefin is selected from the group consisting of isobutylene, propylene trimer, propylene tetramer, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, 1-docosene, 1-tetracosene, and mixtures of the foregoing.

4. The process of claim 2 wherein the olefin is selected from the group consisting of isobutylene, propylene trimer, propylene tetramer, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, 1-docosene, 1-tetracosene, and mixtures of the foregoing.

5. The process of claim 1 wherein said elevated temperature is in the range of from about 120° to about 160° C.

6. The method of claim 1 wherein the olefin comprises a mixture of C 14 –C 18 α-olefins.

7. The method of claim 1 wherein the olefin comprises a blend of C 20 , C 22 , and C 24 α-olefins.

8. The method of claim 1 wherein the olefin comprises propylene pentamer.

9. The method of claim 1 wherein the olefin comprises 2-methyl-1-undecene.

Assignments (3)
CHANGE OF NAME Recorded Sep 25, 2018
From: CROMPTON CORPORATION
To: CHEMTURA CORPORATION
Reel/Frame 047141/0152 →
RELEASE OF FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042447/0508 →
RELEASE OF SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042449/0001 →