ES447999A1 - Synthesis of 2,6-dihydroxycineol - Google Patents

Synthesis of 2,6-dihydroxycineol

Info

Publication number
ES447999A1
ES447999A1 ES447999A ES447999A ES447999A1 ES 447999 A1 ES447999 A1 ES 447999A1 ES 447999 A ES447999 A ES 447999A ES 447999 A ES447999 A ES 447999A ES 447999 A1 ES447999 A1 ES 447999A1
Authority
ES
Spain
Prior art keywords
stage
dihydroxycycloinol
subjecting
synthesis
chloroform
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
ES447999A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CORVI CAMILLO SpA
Original Assignee
CORVI CAMILLO SpA
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 CORVI CAMILLO SpA filed Critical CORVI CAMILLO SpA
Publication of ES447999A1 publication Critical patent/ES447999A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Process for the synthesis of 2,6-dihydroxycycloinol, characterized in that it comprises, in a first step, the subjecting of very pure pinol to bromination in 2,6-dibromocinol with satic acetate and acetic acid; and in a second stage subjecting to hydrolysis, the latter with diluted solution of a mineral acid, such as sulfuric, at about 100ºC according to the following reactions: ** (see formula) ** Obtaining a mass that, in a third stage, is cooled, extracted and washed with chloroform; and in a final stage, the chloroform solution isolates the dihydroxycycloinol by evaporation and crystallization; and additionally because it is acted on an industrial scale. (Machine-translation by Google Translate, not legally binding)
ES447999A 1973-06-12 1976-05-17 Synthesis of 2,6-dihydroxycineol Expired ES447999A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT2512773 1973-06-12

Publications (1)

Publication Number Publication Date
ES447999A1 true ES447999A1 (en) 1977-07-01

Family

ID=11215780

Family Applications (1)

Application Number Title Priority Date Filing Date
ES447999A Expired ES447999A1 (en) 1973-06-12 1976-05-17 Synthesis of 2,6-dihydroxycineol

Country Status (5)

Country Link
JP (1) JPS59122490A (en)
AT (1) AT334348B (en)
BE (1) BE816168A (en)
ES (1) ES447999A1 (en)
FR (1) FR2245355A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112012013299A2 (en) * 2009-12-04 2019-09-24 Commw Scient Ind Res Org polymer, use of a compound, use of a polymer, process for producing a polymer, sheet, fiber or film and polymer blend

Also Published As

Publication number Publication date
JPS6116397B2 (en) 1986-04-30
FR2245355B1 (en) 1977-11-10
JPS59122490A (en) 1984-07-14
FR2245355A1 (en) 1975-04-25
AT334348B (en) 1976-01-10
ATA481474A (en) 1976-05-15
BE816168A (en) 1974-09-30

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