AT57146B - Process for the separation of m- and p-cresol. - Google Patents

Process for the separation of m- and p-cresol.

Info

Publication number
AT57146B
AT57146B AT57146DA AT57146B AT 57146 B AT57146 B AT 57146B AT 57146D A AT57146D A AT 57146DA AT 57146 B AT57146 B AT 57146B
Authority
AT
Austria
Prior art keywords
cresol
separation
mixture
benzene
allowed
Prior art date
Application number
Other languages
German (de)
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Application granted granted Critical
Publication of AT57146B publication Critical patent/AT57146B/en

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

   <Desc/Clms Page number 1> 
 
 EMI1.1 
 
 EMI1.2 
 
 EMI1.3 
 

 <Desc/Clms Page number 2> 

 
 EMI2.1 
 Lösung langsam abkühlen gelassen. Aus der   auskriatallisierten   m-Kresolsulfosäure lässt sich das m-Kresol durch Behandeln mit   überhitztem   Wasserdampf isolieren, während der Benzolextrakt nach dem Abdestillieren des Lösungsmittels ein p-Kresol ergibt, das in der Kälte erstarrt. 



   B e i s pie 111 : 1000 kg des Gemisches von   n-und   p-Kresol werden in 500 kg Benzol gelöst und unter tüchtigem   Rühren   bei etwa 40  950 kg konzentrierter Schwefelsäure hinzufliessen gelassen. Nachdem die Sulfurierung beendet ist, wird unter Umrühren mit Wasser oder verdünnter   Schwefelsäure   verdünnt, das Benzol, das einen Teil des p-Kresols gelöst enthält, abgetrennt und das Sulfurierungsgemisch erkalten gelassen, Auch hier kristallisiert die   m-Kresol-   sulfosäure aus, während die Mutterlauge bei der Spaltung ein   Kresolgemisch ergibt, in welchem   
 EMI2.2 




   <Desc / Clms Page number 1>
 
 EMI1.1
 
 EMI1.2
 
 EMI1.3
 

 <Desc / Clms Page number 2>

 
 EMI2.1
 Solution allowed to cool slowly. The m-cresol can be isolated from the crystallized m-cresol sulfonic acid by treatment with superheated steam, while the benzene extract gives a p-cresol after distilling off the solvent, which solidifies in the cold.



   Example 111: 1000 kg of the mixture of n- and p-cresol are dissolved in 500 kg of benzene and allowed to flow in with about 40,950 kg of concentrated sulfuric acid while stirring vigorously. After the sulfurization has ended, the mixture is diluted with water or dilute sulfuric acid while stirring, the benzene, which contains some of the p-cresol in dissolved form, is separated off and the sulfurization mixture is allowed to cool. Here, too, the m-cresol sulfonic acid crystallizes out while the mother liquor on cleavage results in a cresol mixture in which
 EMI2.2


 

Claims (1)

EMI2.3 EMI2.3
AT57146D 1911-01-25 1911-09-13 Process for the separation of m- and p-cresol. AT57146B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE57146X 1911-01-25

Publications (1)

Publication Number Publication Date
AT57146B true AT57146B (en) 1913-01-10

Family

ID=5629045

Family Applications (1)

Application Number Title Priority Date Filing Date
AT57146D AT57146B (en) 1911-01-25 1911-09-13 Process for the separation of m- and p-cresol.

Country Status (1)

Country Link
AT (1) AT57146B (en)

Similar Documents

Publication Publication Date Title
AT57146B (en) Process for the separation of m- and p-cresol.
AT63818B (en) Process for the preparation of pure meta-cresol.
AT111249B (en) Process for the preparation of complex antimony compounds.
DE499523C (en) Process for the production of ª ‡ -oxy acids from their nitriles
DE604406C (en)
DE444325C (en) Process for the preparation of a naphthalene sulfocarboxylic acid anhydride
DE245892C (en)
DE499823C (en) Process for the preparation of 1-phenyl-2, 3-dimethyl-4-dimethylamino-5-pyrazolone
DE964235C (en) Process for the separation of mixtures of 3, 5- and 3, 4-dichlorotoluene
DE726431C (en) Process for the preparation of arylides from ª ‰ -ketone carboxylic acids
DE386632C (en) Process for resin removal and cleaning of montan wax
DE679279C (en) Process for the preparation of a tetraalkylated dinitrobenzene
AT121246B (en) Process for the deposition of 2-amino-5-iodopyridine.
DE875201C (en) Process for the preparation of substituted aryl vinyl sulfones
DE533470C (en) Process for the preparation of dinaphthocarbazole sulfonic acids and their corresponding oxy compounds
DE542254C (en) Process for the concentration of aqueous formic acid
AT277247B (en) Process for the preparation of the disulfur acid ester salts of 4,4&#39;-DIHYDROXY-DIPHENYL- (2 &#34;-PYRIDYL) -METHANE
DE595604C (en) Process for the production of products with a particularly high emulsifying power from the alkaline refining waste from mineral oils that has been freed from water as far as possible
DE355388C (en) Process for the production of pure phenol free of homologous cresols from coal tar oils
DE496393C (en) Process for the preparation of anthraquinone and its offshoots
AT124276B (en) Process for the production of pure m-cresol or pure m- and p-cresol.
CH124080A (en) Process for the preparation of an organic rhodane compound.
CH242291A (en) Process for the preparation of a p-amino-benzenesulfonamide.
CH142340A (en) Process for the preparation of an arylcarboxamide-o-thioglycolic acid.
CH198707A (en) Process for the preparation of 4,4&#39;-tetramethyldiaminobenzophenone.