CH100352A - Process for the preparation of an aryloxynaphthyl ketone. - Google Patents

Process for the preparation of an aryloxynaphthyl ketone.

Info

Publication number
CH100352A
CH100352A CH100352DA CH100352A CH 100352 A CH100352 A CH 100352A CH 100352D A CH100352D A CH 100352DA CH 100352 A CH100352 A CH 100352A
Authority
CH
Switzerland
Prior art keywords
chloro
ketone
act
aryloxynaphthyl
carboxylic acid
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
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 Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH100352A publication Critical patent/CH100352A/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C65/32—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing keto groups
    • C07C65/40—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing keto groups containing singly bound oxygen-containing groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
    • C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups

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

Description

  

  Verfahren zur Herstellung eines     Aryloxynaphtylketons.       <B>Es</B> wurde gefunden, dass man ein     Aryloxy-          n.aphtylketon    herstellen kann, wenn man auf       1-Oxynaphtalin-2-carbonsäure,    mit oder ohne  Zusatz von     Verdünnungs-        bezw.    Kondensa  tionsmitteln, aber unter Ausschluss von     Alka-          lien,        1-Chlor-2-naphthotrichlorid        einwirken     lässt.

   Die so gewonnene     1-Chlor-2-        1'-dinaph-          tylketon-4'-oxy    -     3'-carbonsäure    bildet weisse  Nadeln, die bei 213   unter Zersetzung schmel  zen und sich in     Atzalkalien    und in konzen  trierter Schwefelsäure mit gelber Farbe lösen.  <I>Beispiel:</I>  28 Teile     1-Chlor-2-naphthotrichlorid    und  <B>18,8</B> Teile 1 -     Oxynaphtalin    - 2 -     carbonsäure     werden bei Zimmertemperatur in 100 Teile  konzentrierter Schwefelsäure eingetragen und  solange zusammen gerührt, bis sich keine Salz  säure mehr entwickelt.

   Hierauf giesst man  in Wasser, filtriert die ausgeschiedene     1-          Chlor-2    .     1'-,dinaphtylketon-4'-oxy-3    -     carbon-          säure    ab und reinigt sie durch     Umkristalli-          sieren    ihres     Natriumsalzes.  



  Process for the preparation of an aryloxynaphthyl ketone. <B> It </B> has been found that an aryloxy n.aphtyl ketone can be produced if one responds to 1-oxynaphthalene-2-carboxylic acid, with or without the addition of diluent or. Condensation agents, but with the exclusion of alkali, allows 1-chloro-2-naphthotrichloride to act.

   The 1-chloro-2- 1'-dinaphthylketone-4'-oxy-3'-carboxylic acid obtained in this way forms white needles which melt at 213 with decomposition and dissolve in caustic alkalis and in concentrated sulfuric acid with a yellow color. <I> Example: </I> 28 parts of 1-chloro-2-naphthotrichloride and <B> 18.8 </B> parts of 1 - oxynaphthalene - 2 - carboxylic acid are added to 100 parts of concentrated sulfuric acid at room temperature and stirred together for as long until no more hydrochloric acid develops.

   It is then poured into water and the 1-chloro-2 which has separated out is filtered off. 1 '-, dinaphthyl ketone-4'-oxy-3 - carboxylic acid and purifies it by recrystallizing its sodium salt.

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Aryloxy- naphtylketons, der 1-Chlor-2- 1'-dinaphtyl- keton-4'-oxy-3'=carbonsäure, dadurch gekenn zeichnet, dass man auf 1-Oxynaphtalin-2-,car- bonsäure unter Ausschluss von Alkalien 1- Chlor-2-naphtotrichlorid einwirken lässt. PATENT CLAIM: Process for the production of an aryloxynaphthyl ketone, the 1-chloro-2- 1'-dinaphthyl-ketone-4'-oxy-3 '= carboxylic acid, characterized in that 1-oxynaphthalene-2-, car- Bonsäure with the exclusion of alkalis 1- chloro-2-naphthotrichloride allows to act. Die 1 - Chlor-2. 1'-dinaphtylketon-4'- oxy-3'- car- bonsäure bildet weisse Nadeln, die bei<B>213'</B> unter Zersetzung schmelzen und sich in Ätz- alkalien und in konzentrierter Schwefelsäure mit gelber Farbe lösen. UNTERANSPRüCHE 1. Verfahren gemäss Patentanspruch, dadurch gekennzeichnet, dass man 1-Chlor-2-naph- totrichlorid mit Zusatz von Verdünnungs mitteln einwirken lässt. 2. The 1 - chlorine-2. 1'-Dinaphtylketon-4'-oxy-3'-carboxylic acid forms white needles, which melt at <B> 213 '</B> with decomposition and dissolve in caustic alkalis and in concentrated sulfuric acid with a yellow color. SUBClaims 1. Process according to claim, characterized in that 1-chloro-2-naphtha trichloride is allowed to act with the addition of diluents. 2. Verfahren gemäss Patentanspruch, dadurch gekennzeichnet, dass man 1-Chlor-2-naph- totrichlorid mit Zusatz von Kondensa tionsmitteln einwirken lässt. Process according to claim, characterized in that 1-chloro-2-naphtha trichloride is allowed to act with the addition of condensation agents.
CH100352D 1921-09-24 1921-09-24 Process for the preparation of an aryloxynaphthyl ketone. CH100352A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH98559T 1921-09-24
CH100352T 1921-09-24

Publications (1)

Publication Number Publication Date
CH100352A true CH100352A (en) 1923-07-16

Family

ID=25705423

Family Applications (1)

Application Number Title Priority Date Filing Date
CH100352D CH100352A (en) 1921-09-24 1921-09-24 Process for the preparation of an aryloxynaphthyl ketone.

Country Status (1)

Country Link
CH (1) CH100352A (en)

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