GB857113A - Manufacture of resorcinol - Google Patents

Manufacture of resorcinol

Info

Publication number
GB857113A
GB857113A GB25567/58A GB2556758A GB857113A GB 857113 A GB857113 A GB 857113A GB 25567/58 A GB25567/58 A GB 25567/58A GB 2556758 A GB2556758 A GB 2556758A GB 857113 A GB857113 A GB 857113A
Authority
GB
United Kingdom
Prior art keywords
resorcinol
steam
distillate
ammonia
aqueous solution
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
GB25567/58A
Inventor
Bernard Hammond Markh Thompson
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB25567/58A priority Critical patent/GB857113A/en
Publication of GB857113A publication Critical patent/GB857113A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/68Purification; separation; Use of additives, e.g. for stabilisation
    • C07C37/70Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
    • C07C37/74Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by distillation
    • C07C37/76Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by distillation by steam distillation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A process for the manufacture of resorcinol by the catalytic cleavage of a reaction mixture containing m-di-isopropylbenzene dihydroperoxide derived from the oxidation of m-diisopropylbenzene, comprises heat decomposing the material less volatile than resorcinol while passing steam through said material, simultaneously distilling off the additional quantities of resorcinol and the m-isopropenyl phenol so formed and recovering the resorcinol from the aqueous distillate while maintaining the pH of the latter at a value of at least 4. The pH may be maintained at a value of at least 4, preferably 4-7, by adding a 30% aqueous solution of ammonium sulphate to the cleavage reaction product so as to bring its pH to about 3. This mixture is then distilled to remove acetone and hydrocarbons and the residual aqueous solution distilled in the presence of steam. During this distillation ammonia formed by dissociation of the ammonium sulphate passes over into the distillate and maintains its pH at at least 4. Alternatively ammonium sulphate or a volatile base such as ammonia or an organic amine may be added to the aqueous solution of resorcinol prior to distillation in the presence of steam, or ammonia may be added directly to the distillate. The maintenance of pH at least 4 is said to reduce the tendency of the m-isopropenyl phenol and resorcinol to combine together to form high boiling by-products. A comparative example is given where an aqueous solution of resorcinol of pH 2,2 is steam-stripped to give an aqueous distillate of pH2,8 and where the solution is first neutralised with ammonia to pH 3,9 and then steam-stripped to given an aqueous distillate of pH 4,9 from which improved yields are recovered.
GB25567/58A 1958-08-08 1958-08-08 Manufacture of resorcinol Expired GB857113A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB25567/58A GB857113A (en) 1958-08-08 1958-08-08 Manufacture of resorcinol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB25567/58A GB857113A (en) 1958-08-08 1958-08-08 Manufacture of resorcinol

Publications (1)

Publication Number Publication Date
GB857113A true GB857113A (en) 1960-12-29

Family

ID=10229785

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25567/58A Expired GB857113A (en) 1958-08-08 1958-08-08 Manufacture of resorcinol

Country Status (1)

Country Link
GB (1) GB857113A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4339614A (en) * 1980-03-14 1982-07-13 Pcuk Produits Chimiques Ugine Kuhlmann Superacid catalyzed preparation of resorcinol from meta-isopropylphenol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4339614A (en) * 1980-03-14 1982-07-13 Pcuk Produits Chimiques Ugine Kuhlmann Superacid catalyzed preparation of resorcinol from meta-isopropylphenol

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