UST861029I4 - Defensive publication - Google Patents

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Publication number
UST861029I4
UST861029I4 US861029DH UST861029I4 US T861029 I4 UST861029 I4 US T861029I4 US 861029D H US861029D H US 861029DH US T861029 I4 UST861029 I4 US T861029I4
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acid
defensive publication
published
application
defensive
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/255Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting
    • C07C51/265Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting having alkyl side chains which are oxidised to carboxyl groups

Definitions

  • High purity phthalic acids such as terephthalic acid are prepared from methyl-substituted benzenes such as p-xylene in solution in aliphatic monocarboxylic acid (e.g., acetic acid) in the presence of cobalt-containing catalyst (e.g., cobalt acetate tetrahydrate) and Without the aid of a promoter, by contacting the reaction mixture, under essentially atmospheric pressure, *with substantially pure molecular oxygen for a period of at least days and preferably at least about 6.5 days, while agitating the reaction mixture and maintaining its temperature at about from to 105 C., and preferably at least C.
  • cobalt-containing catalyst e.g., cobalt acetate tetrahydrate
  • the resulting phthalic acid is collected, e.g., by filtration, washed with aliphatic acid solvent (e.g., acetic acid), and then dried to give (based on the Weight of initial methylswbstituted benzene) at least a 94% yield of phthalic acid (calculated as acid) which acid has a purity of at least about 97% by weight.
  • aliphatic acid solvent e.g., acetic acid

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Description

ft (9 DEFENSIVE PUBLICATION UNITED STATES PATENT OFFICE Published at the request of the applicant or owner in accordance with the Notice of Apr. 11, 1968, 849 O.G. 1221. Identification is by serial number of the application and the heading indicates the number of pages of specification, including claims, and of sheets of drawing contained in the application as originally filed. The file of this application is available to the public for inspection; reproduction may be purchased for '30 cents per sheet.
Applications published under the Defensive Publication Program have not been examined as to the merits of alleged invention. The Patent Ofiice makes no assertion as to the novelty of the disclosed subject matter.
PUBLISHED APRIL 15, 1969 707 405 PREPARATION OF PHTl'iIALIC ACIDS BY SLOW OXIDATION Frederic B. Kirby, 13 Council Trail, Indian Field, Del. 19703 Filed Feb. 23, 1968. Published Apr. 15, 1969 Class 260-524 No Drawing. 13 Pages Specification High purity phthalic acids such as terephthalic acid are prepared from methyl-substituted benzenes such as p-xylene in solution in aliphatic monocarboxylic acid (e.g., acetic acid) in the presence of cobalt-containing catalyst (e.g., cobalt acetate tetrahydrate) and Without the aid of a promoter, by contacting the reaction mixture, under essentially atmospheric pressure, *with substantially pure molecular oxygen for a period of at least days and preferably at least about 6.5 days, while agitating the reaction mixture and maintaining its temperature at about from to 105 C., and preferably at least C. The resulting phthalic acid is collected, e.g., by filtration, washed with aliphatic acid solvent (e.g., acetic acid), and then dried to give (based on the Weight of initial methylswbstituted benzene) at least a 94% yield of phthalic acid (calculated as acid) which acid has a purity of at least about 97% by weight.
US861029D 1968-02-23 1968-02-23 Defensive publication Pending UST861029I4 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US70740568A 1968-02-23 1968-02-23

Publications (1)

Publication Number Publication Date
UST861029I4 true UST861029I4 (en) 1969-04-15

Family

ID=24841562

Family Applications (1)

Application Number Title Priority Date Filing Date
US861029D Pending UST861029I4 (en) 1968-02-23 1968-02-23 Defensive publication

Country Status (6)

Country Link
US (1) UST861029I4 (en)
BE (1) BE728749A (en)
DE (1) DE1908787A1 (en)
FR (1) FR2002471A1 (en)
GB (1) GB1188928A (en)
NL (1) NL6902768A (en)

Also Published As

Publication number Publication date
FR2002471A1 (en) 1969-10-17
GB1188928A (en) 1970-04-22
BE728749A (en) 1969-08-01
DE1908787A1 (en) 1969-09-25
NL6902768A (en) 1969-08-26

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