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US4490570A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for para selective alkylation employing silicalite catalysts

Assignee: Cosden Technology Inc
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Filing: 1982-02-22
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Granted: 1984-12-25
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Expires: 2002-02-22
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Abstract

Abstract A process for the selective alkylation of a monoalkyl benzene in which the alkyl substituent is either methyl or ethyl, to yield a dialkylbenzene product in which the para isomer of the disubstituted product is present in a concentration greater than in a thermodynamic equilibrium is provided. The method essentially comprises passing the monoalkyl benzene and an alkylating agent capable of methylation or ethylation through a reaction zone containing a crystalline silica polymorph silicalite catalyst. Water, in the form of steam, can be co-fed as an option.

Inventors

  • 👤 Cleve H. Forward
  • 👤 James R. Butler
  • 👤 James M. Watson
  • 👤 Gary D. Branum

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 17:49
CPC Classifications
C; C07; C07C; C07C2/00; C07C2/54; C07C2/64; C07C2/66; C07C2529/00; C07C2529/03; C07C2529/035

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 81 words
A process for the selective alkylation of a monoalkyl benzene in which the alkyl substituent is either methyl or ethyl, to yield a dialkyl benzene product in which the para isomer of the disubstituted product is present in a concentration greater than in a thermodynamic equilibrium, comprising: passing the monoalkyl benzene and an alkylating agent capable of methylation or ethylation under conversion conditions which do not include steam cofeed through a reaction zone containing an unmodified crystalline silica polymorph silicalite catalyst.
Claim 2
Dependent Claim 81 words
A process for the selective alkylation of a monoalkyl benzene in which the alkyl substituent is either methyl or ethyl, to yield a dialkyl benzene product in which the para isomer of the disubstituted product is present in a concentration greater than in a thermodynamic equilibrium, comprising: passing the monoalkyl benzene and an alkylating agent capable of methylation or ethylation under conversion conditions which do not include steam cofeed through a reaction zone containing an unmodified crystalline silica polymorph silicalite catalyst.
Claim 3
Dependent Claim 13 words
The process as recited in claim 1 wherein the alkylating agent is ethylene.
Claim 4
Dependent Claim 13 words
The process as recited in claim 1 wherein the monoalkyl benzene is toluene.
Claim 5
Dependent Claim 62 words
The method as recited in claim 1 wherein the conversion conditions comprise temperatures in the range of from about 300° C. to about 600° C., a molar feed ratio of monoalkyl benzene to alkylating agent between about 2:1 to about 20:1, a monoalkyl benzene WHSV ranging from about 50 to about 200 and pressures ranging from about atmospheric to about 25 atmospheres.
Claim 6
Dependent Claim 57 words
The process as recited in claim 4 wherein the temperature range is from about 350° C. to about 450° C., the molar feed ratio range is from about 7:1 to about 18:1, the pressure range is from about 11 atmospheres to about 13 atmospheres and the monoalkyl benzene WHSV range is from about 120 to about 200.
Claim 7
Dependent Claim 80 words
A process for producing dialkyl benzene products comprising: (a) introducing to a reaction zone containing a bed of a crystalline silica polymorph silicalite catalyst a monoalkyl benzene and an alkylating agent; (b) allowing said monoalkyl benzene and alkylating agent to come into contact with said silicalite catalyst material under conversion conditions which do not include steam cofeed; and (c) recovering from said reaction zone a dialkyl benzene isomer mix comprising a greater than thermodynamic equilibrium amount of the para-isomer thereof.
Claim 8
Dependent Claim 80 words
A process for producing dialkyl benzene products comprising: (a) introducing to a reaction zone containing a bed of a crystalline silica polymorph silicalite catalyst a monoalkyl benzene and an alkylating agent; (b) allowing said monoalkyl benzene and alkylating agent to come into contact with said silicalite catalyst material under conversion conditions which do not include steam cofeed; and (c) recovering from said reaction zone a dialkyl benzene isomer mix comprising a greater than thermodynamic equilibrium amount of the para-isomer thereof.

References Cited (Backward Citations)

US4238318A Cited
US4104319A Cited
US4283306A Cited
EP0021475A1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-12-25 1988-06-25 1988-12-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-12-25 1992-06-25 1992-12-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-12-25 1996-06-25 1996-12-25 $7700.00 Window Closed / Lapsed

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