CS274795B2 - Method of 3a-hydroxy-5-diamantanone production - Google Patents

Method of 3a-hydroxy-5-diamantanone production

Info

Publication number
CS274795B2
CS274795B2 CS62190A CS62190A CS274795B2 CS 274795 B2 CS274795 B2 CS 274795B2 CS 62190 A CS62190 A CS 62190A CS 62190 A CS62190 A CS 62190A CS 274795 B2 CS274795 B2 CS 274795B2
Authority
CS
Czechoslovakia
Prior art keywords
hydroxy
diamantanone
optimally
production
ch2oh
Prior art date
Application number
CS62190A
Other languages
Czech (cs)
Other versions
CS62190A2 (en
Inventor
Josef Ing Csc Janku
Ludek Doc Ing Csc Vodicka
Original Assignee
Vysoka Skola Chem Tech
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 Vysoka Skola Chem Tech filed Critical Vysoka Skola Chem Tech
Priority to CS62190A priority Critical patent/CS274795B2/en
Publication of CS62190A2 publication Critical patent/CS62190A2/en
Publication of CS274795B2 publication Critical patent/CS274795B2/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/385—Saturated compounds containing a keto group being part of a ring
    • C07C49/487—Saturated compounds containing a keto group being part of a ring containing hydroxy groups
    • C07C49/507—Saturated compounds containing a keto group being part of a ring containing hydroxy groups polycyclic
    • C07C49/513—Saturated compounds containing a keto group being part of a ring containing hydroxy groups polycyclic a keto group being part of a condensed ring system

Landscapes

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

Abstract

The method of preparation of 3<a>-hydroxy-5-diamantanones of general formula I, where X means H, OH, CH2OH, COOH, consists in the fact that mineral acids are let to treat lactone of 4-hydroxytetracyclo-/7, 3, 1, 0<2>,70<6>, 11/-12-carboxylic acid of general formula II, where X means H, OH, CH2OH, COOH at a temperature of 40 to 200 degrees C, optimally from 100 to 110 degrees C for a period of 1 to 20 hours, optimally from 4 to 8 hours at molar ratio of lactone : mineral acid ranging from 1:2 to 1:100, optimally from 1:10 to 1:20. The 3<a>-hydroxy-5-diamantanone belongs to the group of synthetic immunostimulants.<IMAGE>
CS62190A 1990-02-08 1990-02-08 Method of 3a-hydroxy-5-diamantanone production CS274795B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CS62190A CS274795B2 (en) 1990-02-08 1990-02-08 Method of 3a-hydroxy-5-diamantanone production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CS62190A CS274795B2 (en) 1990-02-08 1990-02-08 Method of 3a-hydroxy-5-diamantanone production

Publications (2)

Publication Number Publication Date
CS62190A2 CS62190A2 (en) 1991-11-12
CS274795B2 true CS274795B2 (en) 1991-11-12

Family

ID=5338638

Family Applications (1)

Application Number Title Priority Date Filing Date
CS62190A CS274795B2 (en) 1990-02-08 1990-02-08 Method of 3a-hydroxy-5-diamantanone production

Country Status (1)

Country Link
CS (1) CS274795B2 (en)

Also Published As

Publication number Publication date
CS62190A2 (en) 1991-11-12

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