GB890387A - Improvements in the production of terephthalic acid - Google Patents

Improvements in the production of terephthalic acid

Info

Publication number
GB890387A
GB890387A GB27989/59A GB2798959A GB890387A GB 890387 A GB890387 A GB 890387A GB 27989/59 A GB27989/59 A GB 27989/59A GB 2798959 A GB2798959 A GB 2798959A GB 890387 A GB890387 A GB 890387A
Authority
GB
United Kingdom
Prior art keywords
oxidation
xylene
acid
mixture
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB27989/59A
Inventor
Walter Speer
Karl Scherf
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB890387A publication Critical patent/GB890387A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/39Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester

Landscapes

  • 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)

Abstract

Terephthalic acid is prepared by oxidising p-xylene with a gas containing molecular oxygen at elevated temperature in the presence of an oxidation catalyst and in the presence of at least 5% by weight of dimethyl terephthalate with reference to the weight of the mixture to be oxidised and at a temperature above the melting point of the diester. The reaction is preferably carried out by passing oxygen through the mixture at 140 DEG C.-200 DEG C. using about 20%-50% of the diester which is said to act as an oxidation promoter and to bring about oxidation to terephthalic acid in one step. The starting material may be pure p-xylene, commercial crude xylene or xylene mixed with partial oxidation products, e.g. tolualdehyde, toluic acid, terephthalaldehydic acid or esters of the acids with alkanols of 1 to 4 carbon atoms. The catalyst may be a copper, cobalt, manganese or cerium salt of a higher aliphatic acid or hydrobromic acid and may be dissolved in the xylene. A lower alkanol, particularly methanol, may be introduced into the oxidation zone during the oxidation in amounts of 0.5% to 5% by weight based on the mixture to be oxidised. The oxidation may be carried out batchwise or continuously at normal or elevated pressures. The product, which may contain some p-toluic acid may be esterified with methanol under increased pressure in a known manner. Examples are given. Specification 623,826 is referred to.
GB27989/59A 1958-08-23 1959-08-17 Improvements in the production of terephthalic acid Expired GB890387A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB50081A DE1076661B (en) 1958-08-23 1958-08-23 Process for the production of isophthalic acid or terephthalic acid or their esters

Publications (1)

Publication Number Publication Date
GB890387A true GB890387A (en) 1962-02-28

Family

ID=6969071

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27989/59A Expired GB890387A (en) 1958-08-23 1959-08-17 Improvements in the production of terephthalic acid

Country Status (2)

Country Link
DE (1) DE1076661B (en)
GB (1) GB890387A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001055073A2 (en) * 2000-01-24 2001-08-02 Basf Aktiengesellschaft Oxidation of o-xylol to produce o-tolyl acid

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001055073A2 (en) * 2000-01-24 2001-08-02 Basf Aktiengesellschaft Oxidation of o-xylol to produce o-tolyl acid
WO2001055073A3 (en) * 2000-01-24 2001-12-20 Basf Ag Oxidation of o-xylol to produce o-tolyl acid

Also Published As

Publication number Publication date
DE1076661B (en) 1960-03-03

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