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US3309410A Expired / Lapsed US ⏱️ 0.0 years remaining

Isomerization process

Assignee: ExxonMobil Technology and Engineering Co
•
Filing: 1964-10-06
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Granted: 1967-03-14
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Expires: 1984-10-06
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Abstract

No abstract record available.

Inventors

  • 👤 Schriesheim Alan
  • 👤 Jr Charles A Rowe

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 19:30
CPC Classifications
C; C07; C07C; C07C5/00; C07C5/22; C07C5/23; C07C5/25; C07C5/2506; C07C5/2562; C07C5/2575

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 116 words
A METHOD OF CONVERTING NONCONJUGATED CYCLIC DIOLEFINS TO CYCLIC CONJUGATED DIOLEFIN ISOMERS WHEREIN BOTH THE NONCONJUGATED AND CONJUGATED DIOLEFINS CONTAIN ONE DOUBLE BOND WITHIN THE CYCLIC STRUCTURE AND ONE DOUBLE BOND ON A SUBSTITUENT SIDE CHAIN, IN HIGH SELECTIVITIES AND YIELDS WHICH COMPRISES MAINTAINING A NONCONJUGATED CYCLIC DIOLEFIN IN CONTRACT WITH A BASE-SOLVENT SYSTEM WHEREIN SAID SOLVENT IS AN APROTIC, DIPOLAR, NONHYDROXYLIC ORGANIC LIQUID HAVING A DIELECTRIC CONSTANT IN EXCESS OF 15 DEBYES AT 25*C. AND SAID BASE IS SELECTED FROM THE GROUP CONSISTING OF ALKALI METAL HYDRIDES, INORGANIC AMIDES, ALKOXIDES, HYDROXIDES, AND ALKYLS AT TEMPERATURES OF FROM ABOUT 10 TO 300*C. AND FOR A PERIOD SUFFICIENT TO CONVERT THE SAME PRINCIPALLY TO CONJUGATED DIOLEFIN ISOMERS.
Claim 2
Independent Claim 116 words
A METHOD OF CONVERTING NONCONJUGATED CYCLIC DIOLEFINS TO CYCLIC CONJUGATED DIOLEFIN ISOMERS WHEREIN BOTH THE NONCONJUGATED AND CONJUGATED DIOLEFINS CONTAIN ONE DOUBLE BOND WITHIN THE CYCLIC STRUCTURE AND ONE DOUBLE BOND ON A SUBSTITUENT SIDE CHAIN, IN HIGH SELECTIVITIES AND YIELDS WHICH COMPRISES MAINTAINING A NONCONJUGATED CYCLIC DIOLEFIN IN CONTRACT WITH A BASE-SOLVENT SYSTEM WHEREIN SAID SOLVENT IS AN APROTIC, DIPOLAR, NONHYDROXYLIC ORGANIC LIQUID HAVING A DIELECTRIC CONSTANT IN EXCESS OF 15 DEBYES AT 25*C. AND SAID BASE IS SELECTED FROM THE GROUP CONSISTING OF ALKALI METAL HYDRIDES, INORGANIC AMIDES, ALKOXIDES, HYDROXIDES, AND ALKYLS AT TEMPERATURES OF FROM ABOUT 10 TO 300*C. AND FOR A PERIOD SUFFICIENT TO CONVERT THE SAME PRINCIPALLY TO CONJUGATED DIOLEFIN ISOMERS.

References Cited (Backward Citations)

US3213155A Cited
US3217050A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1970-03-13 1970-09-12 1971-03-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1974-03-13 1974-09-12 1975-03-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1978-03-13 1978-09-12 1979-03-14 $7700.00 Window Closed / Lapsed

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