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US3997569A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for preparing a lactone reaction product

Assignee: Texaco Inc
•
Filing: 1974-02-28
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Granted: 1976-12-14
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Expires: 1994-02-28
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Abstract

Abstract Method for preparing a lactone reaction product comprising reacting an alkenylsuccinic acid under substantially anhydrous conditions in the presence of a protonating agent and at an elevated temperature ranging up to about 100° C., and a motor fuel composition containing said lactone reaction product.

Inventors

  • 👤 Justin Christopher Powell

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 08:06
CPC Classifications
C; C08; C08F; C08F8/00

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 111 words
A method for preparing a high molecular weight alkenyl-substituted lactone reaction product comprising the step of admixing an alkenylsuccinic acid, said alkenyl radical having an average molecular weight ranging from about 300 to 3,000 with a protonating agent or electron pair acceptor selected from the group consisting of sulfuric acid, perchloric acid, p-toluene sulfonic acid, boron trifluoride etherate and sulfonic acid ion exchange resins to form a substantially anhydrous reaction mixture and reacting said mixture under substantially anhydrous reaction conditions at an elevated temperature up to about 100° C until infrared spectra at about 5.66 and 5.74 micrometers indicates a substantial conversion of said alkenyl-succinic acid to said lactone reaction product.
Claim 2
Independent Claim 111 words
A method for preparing a high molecular weight alkenyl-substituted lactone reaction product comprising the step of admixing an alkenylsuccinic acid, said alkenyl radical having an average molecular weight ranging from about 300 to 3,000 with a protonating agent or electron pair acceptor selected from the group consisting of sulfuric acid, perchloric acid, p-toluene sulfonic acid, boron trifluoride etherate and sulfonic acid ion exchange resins to form a substantially anhydrous reaction mixture and reacting said mixture under substantially anhydrous reaction conditions at an elevated temperature up to about 100° C until infrared spectra at about 5.66 and 5.74 micrometers indicates a substantial conversion of said alkenyl-succinic acid to said lactone reaction product.
Claim 3
Dependent Claim 40 words
A process according to claim 1 in which the concentration of said protonating agent or electron pair acceptor is sufficient to provide from about 0.25 to 1.5 moles of protons or electron pair acceptors per mole of said alkenylsuccinic acid.
Claim 4
Dependent Claim 40 words
A method according to claim 1 in which the concentration of said protonating agent or electron pair acceptors is sufficient to provide from about 0.5 to 1 moles of protons or electron pair acceptors per mole of said alkenyl-succinic acid.
Claim 5
Dependent Claim 22 words
A method according to claim 1 in which the average molecular weight of said alkenyl radical ranges from about 700 to 2,000.
Claim 6
Dependent Claim 22 words
A method according to claim 1 in which the average molecular weight of said alkenyl radical ranges from about 800 to 1200.
Claim 7
Dependent Claim 15 words
A method according to claim 1 in which said protonating agent is concentrated sulfuric acid.
Claim 8
Dependent Claim 16 words
A method according to claim 6 in which said protonating agent is 96 percent sulfuric acid.
Claim 9
Dependent Claim 22 words
A method according to claim 1 in which said reaction is conducted at a temperature ranging from about 60° to 100° C.
Claim 10
Dependent Claim 22 words
A method according to claim 1 in which said reaction is conducted at a temperature ranging from about 90° to 99° C.
Claim 11
Dependent Claim 23 words
A method according to claim 1 in which equimolar amounts of an alkenylsuccinic anhydride and water are reacted to form said alkenylsuccinic acid.
Claim 12
Dependent Claim 18 words
A method according to claim 1 in which said reaction mixture is dissolved in an inert hydrocarbon solvent.
Claim 13
Dependent Claim 14 words
A method according to claim 11 in which said solvent is a mineral oil.
Claim 14
Dependent Claim 37 words
A method according to claim 1 in which infrared radiation absorption characteristics of lactone at about 5.61 and 5.74 micrometers indicates the conversion of at least 50 percent of said alkenylsuccinic acid to said lactone reaction product.
Claim 15
Dependent Claim 18 words
A method according to claim 1 in which said reaction mixture contains less than about 5 percent water.
Claim 16
Dependent Claim 18 words
A method according to claim 1 in which said reaction mixture contains less than about 2 percent water.
Claim 17
Dependent Claim 22 words
A method according to claim 1 in which said alkenyl radical has an average molecular weight ranging from about 1,000 to 3,000.
Claim 18
Dependent Claim 22 words
A method according to claim 13 in which the yield of lactones from said alkenylsuccinic acid is greater than 85 mole percent.

References Cited (Backward Citations)

US3155686A Cited
US3155685A Cited
US3267062A Cited
US3755173A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-12-14 1980-06-14 1980-12-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-12-14 1984-06-14 1984-12-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-12-14 1988-06-14 1988-12-14 $7700.00 Window Closed / Lapsed

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