FR2098755A5 - Mevalolactone and its homologues - prepd from 4-hydroxy-2-butanone and an acid - Google Patents

Mevalolactone and its homologues - prepd from 4-hydroxy-2-butanone and an acid

Info

Publication number
FR2098755A5
FR2098755A5 FR7027582A FR7027582A FR2098755A5 FR 2098755 A5 FR2098755 A5 FR 2098755A5 FR 7027582 A FR7027582 A FR 7027582A FR 7027582 A FR7027582 A FR 7027582A FR 2098755 A5 FR2098755 A5 FR 2098755A5
Authority
FR
France
Prior art keywords
acid
mevalolactone
prepd
butanone
hydroxy
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
FR7027582A
Other languages
French (fr)
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.)
LAIRE PRODUITS CHIMIE
Original Assignee
LAIRE PRODUITS CHIMIE
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 LAIRE PRODUITS CHIMIE filed Critical LAIRE PRODUITS CHIMIE
Priority to FR7027582A priority Critical patent/FR2098755A5/en
Application granted granted Critical
Publication of FR2098755A5 publication Critical patent/FR2098755A5/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/16Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D309/28Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/30Oxygen atoms, e.g. delta-lactones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/10Oxygen atoms
    • C07D309/12Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Mevalolactone (I) and other lactones with the same nuclear skeleton are prepd. by reaction of 4-hydroxy-2-butanone (II) or a higher homologue, with an aliphatic acid of >=2C atoms, an aryl aliphatic acid or a cycloaliphatic acid, in the presence of Li, Na or K and an aromatic solvent having >=2 rings. The mevalonic acid produced is converted into (I) by dilute acid. (I) is a precursor in the biosynthesis of steroids.
FR7027582A 1970-07-27 1970-07-27 Mevalolactone and its homologues - prepd from 4-hydroxy-2-butanone and an acid Expired FR2098755A5 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
FR7027582A FR2098755A5 (en) 1970-07-27 1970-07-27 Mevalolactone and its homologues - prepd from 4-hydroxy-2-butanone and an acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7027582A FR2098755A5 (en) 1970-07-27 1970-07-27 Mevalolactone and its homologues - prepd from 4-hydroxy-2-butanone and an acid

Publications (1)

Publication Number Publication Date
FR2098755A5 true FR2098755A5 (en) 1972-03-10

Family

ID=9059284

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7027582A Expired FR2098755A5 (en) 1970-07-27 1970-07-27 Mevalolactone and its homologues - prepd from 4-hydroxy-2-butanone and an acid

Country Status (1)

Country Link
FR (1) FR2098755A5 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2392016A1 (en) * 1977-05-24 1978-12-22 Sankyo Co MEVALONOLACTONE DERIVATIVES, THEIR PREPARATION PROCESS AND THEIR THERAPEUTIC APPLICATION

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2392016A1 (en) * 1977-05-24 1978-12-22 Sankyo Co MEVALONOLACTONE DERIVATIVES, THEIR PREPARATION PROCESS AND THEIR THERAPEUTIC APPLICATION

Similar Documents

Publication Publication Date Title
JPS5265259A (en) Synthesis of 16beta-alkylestradiol or its 17-esters
FR2098755A5 (en) Mevalolactone and its homologues - prepd from 4-hydroxy-2-butanone and an acid
GB943078A (en) Process for the preparation of riboflavin tetrabutyrate
CA921934A (en) Preparation of a phenol from a benzenemonocarboxylic acid
GB1335930A (en) Macrocyclic compounds and processes for their preparation
AU457146B2 (en) Method of manufacture ofan acid compound with controlled release
JPS522095A (en) Emergency escapement apparatus for guilding
IL36213A (en) 3-oxo-13beta-alkyl-17alpha-methyl-20(alpha or beta)-hydroxy-19-nor or 18,19-dinorpregna-4,9-dienes and process of preparation
GB1323494A (en) Methylene-bis-chlorophenol
GB1413956A (en) Total steroid synthesis via a-norsteroids
GB1164705A (en) Preparation of Delta<7>-Dehydro Steroids
CA622899A (en) METHOD OF PREPARING TEREPHTHALIC ACID ESTERS FROM .alpha.,.alpha.,.alpha.,.alpha.',.alpha.',.alpha.'-HEXACHLORO-P-XYLENE
CA972350A (en) 1,2-METHYLENE-17.alpha.-ACYLOXY(OR IMPROVED HYDROXY)-9.beta.,10.alpha.-STEROID COMPOUNDS OF THE PREGNANE SERIES, PHARMACEUTIC PREPARATIONS OF THE BASIS OF THE NOVEL COMPOUNDS AND METHODS OF PRODUCING SAID COMPOUNDS AND PREPARATIONS
JPS5242339A (en) Micro instruction address production system
FR2100033A5 (en) 2-hydroxynaphthalene-3-carboxylic acid - from beta-naphthol in presen of diphenyl (oxide) and/or alkylnaphthalene
CA835959A (en) PREPARATION OF ESTERS OF .alpha.,.alpha.'-DIMETHYLMUCONIC ACID
VENINI Relativistic behavior of an observer in uniformly accelerated translational motion relative to an inertial observer(Relativistic behavior of uniformly accelerated translational observer motion relative to inertial observer from space-time transformation)
AU450333B2 (en) Preparation of o,o-dimethhyl-thiono phosphoric acid [o-quinoxalyl-(2)ester
CA698201A (en) PROCESS OF PRODUCING .alpha.-CHLOROGLUTARIC ACID
CA602214A (en) POLYMERS OF 4 (.beta.-HYDROXY-ETHOXY)-3-METHYLBENZOIC ACID
CA595836A (en) METHOD OF PRODUCING 11 (.alpha.) HYDROXYSTEROIDS
CA603561A (en) HALOARYLOXYALKYL ESTERS OF .alpha.,.alpha.-DICHLOROBUTYRIC ACID
AU259089B2 (en) Production of l-glulamic acid from aerobic fermentation of carbohydrates
AU260719B2 (en) Process for preparation of polyesters by reaction ofan anhydride witha cyclic ester, and products thereof
GB1030389A (en) Resolution of organic acid

Legal Events

Date Code Title Description
TP Transmission of property
ST Notification of lapse