Continuous adiabatic process for the mononitration of benzene
First Claim
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1. In an adiabatic process for the mononitration of benzene with nitric acid to produce mononitrobenzene, whereby a reactant stream of benzene and a reactant stream of a mixed acid comprising nitric acid, sulfuric acid and water are contacted at an elevated temperature to produce a nitration reaction mixture;
- whereby the heat of mixing and heat of reaction produced thereby is absorbed by said reaction mixture and utilized therein in the nitration reaction;
whereby the product of the reaction, consisting of an organic phase containing said mononitrobenzene and an aqueous phase consisting essentially of hot aqueous sulfuric acid are separated; and
whereby said organic phase is washed free of acidic by-products to yield said mononitrobenzene, the improvement which comprises;
contacting a reactant stream of a stoichiometric excess of benzene and a reactant stream of a mixed acid, comprising from about 3 to 7.5 percent by weight of nitric acid, from about 58.5 to 66.5 percent by weight of sulfuric acid and from about 28 to 37 percent by weight of water, to form a nitration reaction mixture at a temperature in the range of from about 80°
C to 120°
C under superatmospheric pressure sufficient to maintain said benzene in said reaction mixture in the liquid state;
subjecting said reaction mixture to vigorous agitation for a period of time sufficient to convert substantially all of said nitric acid to mononitrobenzene;
separating said reaction product composition, at a temperature not in excess of about 145°
C, into an organic phase and an aqueous sulfuric acid phase, said aqueous sulfuric acid phase containing essentially no nitric acid and comprising from about 62 to 68 percent by weight of sulfuric acid; and
recovering said mononitrobenzene from said organic phase, said mononitrobenzene being characterized as containing less than about 500 parts per million of dinitrobenzene.
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Abstract
Benzene is admixed and reacted continuously with a mixed acid containing 3-7.5% nitric acid, 58.5-66.5% sulfuric acid, and 28-37% water under pressure sufficient to maintain benzene in liquid state until complete conversion of nitric acid is achieved to provide mononitrobenzene containing less than 500 ppm dinitrobenzene.
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Citations
3 Claims
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1. In an adiabatic process for the mononitration of benzene with nitric acid to produce mononitrobenzene, whereby a reactant stream of benzene and a reactant stream of a mixed acid comprising nitric acid, sulfuric acid and water are contacted at an elevated temperature to produce a nitration reaction mixture;
- whereby the heat of mixing and heat of reaction produced thereby is absorbed by said reaction mixture and utilized therein in the nitration reaction;
whereby the product of the reaction, consisting of an organic phase containing said mononitrobenzene and an aqueous phase consisting essentially of hot aqueous sulfuric acid are separated; and
whereby said organic phase is washed free of acidic by-products to yield said mononitrobenzene, the improvement which comprises;
contacting a reactant stream of a stoichiometric excess of benzene and a reactant stream of a mixed acid, comprising from about 3 to 7.5 percent by weight of nitric acid, from about 58.5 to 66.5 percent by weight of sulfuric acid and from about 28 to 37 percent by weight of water, to form a nitration reaction mixture at a temperature in the range of from about 80°
C to 120°
C under superatmospheric pressure sufficient to maintain said benzene in said reaction mixture in the liquid state;
subjecting said reaction mixture to vigorous agitation for a period of time sufficient to convert substantially all of said nitric acid to mononitrobenzene;
separating said reaction product composition, at a temperature not in excess of about 145°
C, into an organic phase and an aqueous sulfuric acid phase, said aqueous sulfuric acid phase containing essentially no nitric acid and comprising from about 62 to 68 percent by weight of sulfuric acid; and
recovering said mononitrobenzene from said organic phase, said mononitrobenzene being characterized as containing less than about 500 parts per million of dinitrobenzene. - View Dependent Claims (2, 3)
- whereby the heat of mixing and heat of reaction produced thereby is absorbed by said reaction mixture and utilized therein in the nitration reaction;
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Current AssigneeAmerican Cyanamid Co (Pfizer Inc.)
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Original AssigneeAmerican Cyanamid Co (Pfizer Inc.)
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InventorsAlexanderson, Verner, Vanderwaart, Cornelius Marsden, Trecek, James Bryan
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Primary Examiner(s)Sebastian, Leland A.
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Application NumberUS05/826,208Time in Patent Office277 DaysField of Search260/645, 203/12, 203/88US Class Current568/939CPC Class CodesC07C 201/08 by substitution of hydrogen...C07C 205/06 having nitro groups bound t...
