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US3248443A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for alkylating aromatic hydrocarbons

Assignee: Monsanto Co
•
Filing: 1963-01-31
•
Granted: 1966-04-26
•
Expires: 1983-01-31
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Abstract

No abstract record available.

Inventors

  • 👤 Gilbert J Mcewan
  • 👤 Sidney G Clark

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 17:52
CPC Classifications
C; C07; C07C; C07C2/00; C07C2/54; C07C2/64; C07C2/66; C07C2/68; C07C2527/00; C07C2527/06; C07C2527/08; C07C2527/12; C07C2527/1213; C07C2527/125; C07C2527/126; C07C2531/00; C07C2531/02

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 123 words
IN AN ALKYLATION PROCESS FOR PRODUCING STRAINGT CHAIN ALKYL ARYL COMPOUNDS WHEREIN THE AROMATIC NUCLEI OF THE AROMATIC COMPOUNDS ARE ALKYLATED USING STRAIGHT CHAIN OLEFINS, THE IMPROVEMENT WHICH COMPRISES ALKYLATING STRAIGHT CHAIN OLEFINS CONTAINING NOT MORE THAN ABOUT 50% BY WEIGHT OF ALPHA OLEFINS WITH AROMATIC COMPOUNDS IN THE PRESENCE OF ALKYLATION CATALYST COMBINATION OF A FRIEDEL-CRAFTS CATALYST SELECTED FROM THE CLASS CONSISTING OF ACTIVATED ALUMINUM CHLORIDE, ACTIVATED ALUMINUM BROMIDE, AND BORON TRIFLUORIDE, AND AN ORGANO-NITRO CATALYST MODIFIER, SAID ALKYLATION CONDUCTED WITH A CATALYST COMBINATION TO OLEFIN MOLAR OF AT LEAST ABOUT 2:1, WHEREBY THE RESULTING STRAIGHT CHAIN ALKYL ARYL COMPOUNDS CONTAIN A RELATIVELY LOW PROPORTION OF THE ISOMER WHEREIN THE ARYL NUCLEUS IN ATTACHED AT THE TWO POSITION OF THE ALKYL CHAIN.
Claim 2
Dependent Claim 123 words
IN AN ALKYLATION PROCESS FOR PRODUCING STRAINGT CHAIN ALKYL ARYL COMPOUNDS WHEREIN THE AROMATIC NUCLEI OF THE AROMATIC COMPOUNDS ARE ALKYLATED USING STRAIGHT CHAIN OLEFINS, THE IMPROVEMENT WHICH COMPRISES ALKYLATING STRAIGHT CHAIN OLEFINS CONTAINING NOT MORE THAN ABOUT 50% BY WEIGHT OF ALPHA OLEFINS WITH AROMATIC COMPOUNDS IN THE PRESENCE OF ALKYLATION CATALYST COMBINATION OF A FRIEDEL-CRAFTS CATALYST SELECTED FROM THE CLASS CONSISTING OF ACTIVATED ALUMINUM CHLORIDE, ACTIVATED ALUMINUM BROMIDE, AND BORON TRIFLUORIDE, AND AN ORGANO-NITRO CATALYST MODIFIER, SAID ALKYLATION CONDUCTED WITH A CATALYST COMBINATION TO OLEFIN MOLAR OF AT LEAST ABOUT 2:1, WHEREBY THE RESULTING STRAIGHT CHAIN ALKYL ARYL COMPOUNDS CONTAIN A RELATIVELY LOW PROPORTION OF THE ISOMER WHEREIN THE ARYL NUCLEUS IN ATTACHED AT THE TWO POSITION OF THE ALKYL CHAIN.

References Cited (Backward Citations)

US2734930A Cited
US2363824A Cited
US2403672A Cited
US2404340A Cited
US2631172A Cited
US2712530A Cited
US2695326A Cited
US2761000A Cited
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US3169987A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1969-04-25 1969-10-25 1970-04-26 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1973-04-25 1973-10-25 1974-04-26 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1977-04-25 1977-10-25 1978-04-26 $7700.00 Window Closed / Lapsed

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