CH100355A - Process for the preparation of an aryloxynaphthyl ketone. - Google Patents

Process for the preparation of an aryloxynaphthyl ketone.

Info

Publication number
CH100355A
CH100355A CH100355DA CH100355A CH 100355 A CH100355 A CH 100355A CH 100355D A CH100355D A CH 100355DA CH 100355 A CH100355 A CH 100355A
Authority
CH
Switzerland
Prior art keywords
ketone
benzotrichloride
act
allowed
aryloxynaphthyl
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 CH100355A publication Critical patent/CH100355A/en

Links

Classifications

    • 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
    • C07C49/83—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups polycyclic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/008—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with tri- or tetrahalomethyl compounds
    • 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

Landscapes

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

Description

  

  verfahren zur Herstellung eines     Aryloxynaphtylketons.       Es wurde gefunden, dass man ein     Aryloxy-          na.plity        llzeton    herstellen kann, wenn man auf       ss-Naplithol,    mit oder ohne Zusatz von     Ver-          dünnunl;s-        bezw.        Kondensationsmitteln,    aber  unter Ausschluss von     Alkalien,        Belizotriehlo-          rid        einwirken    lässt.

   Das so gewonnene 1 .     1'-          PhenyInaplity    1 - 2'-     oxy    -     keton    bildet weisse  Nadeln,     !die    bei 175   schmelzen und sich in       Ätzalkalien    und in konzentrierter Schwefel  säure mit gelber Farbe lösen.         Beispiel:            19,,i.    Teile     Benzotrichlorid    und 14,4 Teile       ss-Nalilitliol    werden unter Kühlung in 100  Teile konzentrierte Schwefelsäure eingetra  gen und so lange zusammen gerührt, bis sich  keine Salzsäure mehr entwickelt.

   Hierauf  giesst man in Wasser, filtriert das ausge  schiedene 1 .     l.'-Plienylnaphtyl    -     2'-oxy-keton     ab und .reinigt es durch     Umkristallisieren     seines     Natriumsalzes.  



  process for the production of an aryloxynaphthyl ketone. It has been found that an aryloxyna.plity llteton can be produced by using ss-naplithol, with or without the addition of thinner or thinner. Condensation agents, but with the exclusion of alkalis, allows belizotri chloride to act.

   The 1. 1'- PhenyInaplity 1 - 2'- oxy - ketone forms white needles! Which melt at 175 and dissolve in caustic alkalis and in concentrated sulfuric acid with a yellow color. Example: 19,, i. Parts of benzotrichloride and 14.4 parts of ß-nalilitliol are introduced into 100 parts of concentrated sulfuric acid with cooling and stirred together until hydrochloric acid no longer develops.

   It is then poured into water, the precipitated 1 is filtered off. l'-Plienylnaphtyl - 2'-oxy-ketone and purifies it by recrystallizing its sodium salt.

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Arylogy- n aphtylketons, des 1.1'- Phenylnaphtyl - 2'- oxy-ketons, dadurch gekennzeichnet, dass man auf- ss-Naphthol unter Ausschluss von Alka- lien Benzotrichlorid einwirken lässt. PATENT CLAIM: Process for the production of an arylogynaphtylketons, the 1,1'-phenylnaphthyl-2'-oxy-ketone, characterized in that benzotrichloride is allowed to act on ß-naphthol with the exclusion of alkali. Das 1 . 1'- Phenylna.phtyl - 2'- oxy - keton bildet weisse Nadeln, die bei 175 schmelzen und sich in Ätzalkalien und in konzentrierter Schwefel säure mit gelber Farbe lösen. <B>UNTERANSPRÜCHE:</B> 1. Verfahren gemäss Patentanspruch, dadurch gekennzeichnet, dass man Benzotrichlorid mit Zusatz von Verdünnungsmitteln ein wirken lässt. 2. Verfahren gemäss Patentanspruch, dadurch gekennzeichnet, dass man Benzotrichlorid mit Zusatz von Kondensationsmitteln ein wirken lässt. The 1st 1'- Phenylna.phtyl - 2'- oxy - ketone forms white needles which melt at 175 and dissolve in caustic alkalis and in concentrated sulfuric acid with a yellow color. SUBClaims: 1. Method according to claim, characterized in that benzotrichloride is allowed to act with the addition of diluents. 2. The method according to claim, characterized in that benzotrichloride is allowed to act with the addition of condensing agents.
CH100355D 1921-09-24 1921-09-24 Process for the preparation of an aryloxynaphthyl ketone. CH100355A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH98559T 1921-09-24
CH100355T 1921-09-24

Publications (1)

Publication Number Publication Date
CH100355A true CH100355A (en) 1923-07-16

Family

ID=25705426

Family Applications (1)

Application Number Title Priority Date Filing Date
CH100355D CH100355A (en) 1921-09-24 1921-09-24 Process for the preparation of an aryloxynaphthyl ketone.

Country Status (1)

Country Link
CH (1) CH100355A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3526666A (en) * 1968-01-12 1970-09-01 Ferro Corp Synthesis of 2-hydroxy-4-alkoxybenzophenones

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3526666A (en) * 1968-01-12 1970-09-01 Ferro Corp Synthesis of 2-hydroxy-4-alkoxybenzophenones

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