CH206038A - Process for preparing a tetrahydronaphthoquinol derivative. - Google Patents

Process for preparing a tetrahydronaphthoquinol derivative.

Info

Publication number
CH206038A
CH206038A CH206038DA CH206038A CH 206038 A CH206038 A CH 206038A CH 206038D A CH206038D A CH 206038DA CH 206038 A CH206038 A CH 206038A
Authority
CH
Switzerland
Prior art keywords
tetrahydronaphthoquinol
derivative
preparing
water
parts
Prior art date
Application number
Other languages
French (fr)
Inventor
Asahina Yasuhiko
Original Assignee
Asahina Yasuhiko
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 Asahina Yasuhiko filed Critical Asahina Yasuhiko
Publication of CH206038A publication Critical patent/CH206038A/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Description

  

  Procédé de préparation d'un dérivé du     tétrahydronaphtoquinol.       L'objet de la présente     invention    est un  procédé de préparation d'un dérivé du     tétra-          hydronaphtoquinol,    suivant lequel on traite  du     tétrahydronaphtoquinol    avec un agent       -d'acétylation,    pour obtenir     l'ester        acétique    -du       tétrahydronaphtoquinol,    lequel   est un pro  duit nouveau à effet     anthelminthique.     



  La substance de départ,. le     tétrahydro-          naphtoquinol    (dont la     préparation    est     -décrite     dans le brevet no 204646) est, elle aussi, un  produit à effet     anthelminthique,    mais sui  vant les     expériences    du demandeur, le produit       acétylé        présente    un effet     anthelminthique     plus efficace que le produit non     acétylé.     Comme agent     -d'acétylation    on peut employer,  par exemple, le chlorure     acétylique,    l'acide  acétique     glacial,

      l'acide     acétique.     



  L'exemple suivant illustre le procédé, les       parties    étant en     poids:     Un mélange de 30     parties    -de     tétrahydro-          naphtoquinol,    30 parties     d'acétate    ,de     sodium     anhydre et 90 parties d'anhydride acétique est       porté    à l'ébullition pendant 1 à 11/2 heure,    une quantité d'eau y étant ajoutée pour hy  drolyser l'anhydride acétique. Le liquide est  ensuite     décoloré    au moyen de charbon de bois  et une nouvelle     quantité    de 200 à 300 par  ties d'eau     est    ajoutée au liquide.  



  Le liquide est alors secoué     plusieurs    fois  de suite chaque fois avec une quantité d'é  ther frais. Tous les extraits éthérés sont     r6u-          nis    et l'eau y contenue en est éliminée. La  solution est subséquemment concentrée par  évaporation et -de l'éther de pétrole y est  ajouté,     ce    qui a pour effet qu'il se forme  un     précipité    cristallin qui est     recristallisé    au  moyen d'eau éthérée ou d'un mélange     d'è-          ther    et d'éther -de pétrole.  



  Le produit obtenu est l'ester acétique du       tétrahy.dronaphtoquinol    -d'un rendement de  25     @à    30 parties.     Il    est incolore et se     mani-          feste    sous une forme cristalline qui peut va  rier. Il est facilement soluble dans l'éther,  l'alcool et le benzène, mais difficilement so  luble dans l'eau. Son point de     fusion    est à       80 -81     C.



  Process for preparing a tetrahydronaphthoquinol derivative. The object of the present invention is a process for the preparation of a derivative of tetrahydronaphthoquinol, according to which tetrahydronaphthoquinol is treated with an acetylating agent, to obtain the acetyl ester of tetrahydronaphthoquinol, which is a product. again with anthelmintic effect.



  The starting substance ,. tetrahydronaphthoquinol (the preparation of which is described in patent No. 204646) is also a product with an anthelmintic effect, but according to the experiences of the applicant, the acetylated product exhibits a more effective anthelmintic effect than the non-acetylated product . As acetylating agent can be used, for example, acetyl chloride, glacial acetic acid,

      acetic acid.



  The following example illustrates the process, the parts being by weight: A mixture of 30 parts of tetrahydronaphthoquinol, 30 parts of acetate, of anhydrous sodium and 90 parts of acetic anhydride is brought to the boil for 1 to 11/2 hour, a quantity of water being added thereto to hydrolysate the acetic anhydride. The liquid is then decolorized with charcoal and a further 200-300 parts water is added to the liquid.



  The liquid is then shaken several times in a row each time with a quantity of fresh ether. All the ethereal extracts are combined and the water contained therein is removed. The solution is subsequently concentrated by evaporation and petroleum ether is added thereto, which causes a crystalline precipitate to form which is recrystallized using ethereal water or a mixture of ether. ther and petroleum ether.



  The product obtained is the acetate ester of tetrahydronaphthoquinol in a yield of 25% to 30 parts. It is colorless and manifests itself in a crystalline form which may laugh. It is easily soluble in ether, alcohol and benzene, but hardly soluble in water. Its melting point is at 80 -81 C.

 

Claims (1)

REVENDICATION Procédé de préparation d'un dérivé du tétrahydronaphtoquinol à effet a.nthelmin- thique, suivant lequel on traite du tétrahy- dronaphtoquinol avec un agent d'acéty lation. L'ester acétique du tétrahydronaphtoqui- nol obtenu est incolore et se manifeste sous une forme cristalline qui peut varier. Il est facilement soluble dans l'éther, l'alcool et le benzène, mais difficilement soluble dans l'eau. Son point de fusion est à 80 -81 C. CLAIM A process for the preparation of a tetrahydronaphthoquinol derivative with an a.nthelmintic effect, according to which tetrahydronaphthoquinol is treated with an acetylating agent. The acetate ester of the obtained tetrahydronaphthoquinol is colorless and manifests itself in a crystalline form which may vary. It is easily soluble in ether, alcohol and benzene, but hardly soluble in water. Its melting point is at 80 -81 C.
CH206038D 1937-10-30 1938-04-22 Process for preparing a tetrahydronaphthoquinol derivative. CH206038A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP206038X 1937-10-30

Publications (1)

Publication Number Publication Date
CH206038A true CH206038A (en) 1939-07-15

Family

ID=12031836

Family Applications (1)

Application Number Title Priority Date Filing Date
CH206038D CH206038A (en) 1937-10-30 1938-04-22 Process for preparing a tetrahydronaphthoquinol derivative.

Country Status (1)

Country Link
CH (1) CH206038A (en)

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