GB1009916A - Improvements in or relating to ª‡-substituted propionaldehydes and process for theirproduction - Google Patents

Improvements in or relating to ª‡-substituted propionaldehydes and process for theirproduction

Info

Publication number
GB1009916A
GB1009916A GB5161/65A GB516165A GB1009916A GB 1009916 A GB1009916 A GB 1009916A GB 5161/65 A GB5161/65 A GB 5161/65A GB 516165 A GB516165 A GB 516165A GB 1009916 A GB1009916 A GB 1009916A
Authority
GB
United Kingdom
Prior art keywords
formula
chlorobenzyl
theirproduction
relating
resin
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
GB5161/65A
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.)
SIMES
SIMES Societa Italiana Medicinali e Sintetici SpA
Original Assignee
SIMES
SIMES Societa Italiana Medicinali e Sintetici 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 SIMES, SIMES Societa Italiana Medicinali e Sintetici SpA filed Critical SIMES
Priority to GB5161/65A priority Critical patent/GB1009916A/en
Publication of GB1009916A publication Critical patent/GB1009916A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • C07C41/18Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/30Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/511Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00Compounds having —CHO groups
    • C07C47/20Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/24Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated

Abstract

The invention comprises aldehydes of formula CH3CHRCHO, wherein R is a p-chlorophenyl, p-chlorobenzyl, o-chlorobenzyl, p-fluorobenzyl or cyclopentyl group, and the preparation thereof and of compounds in which R is an isopropyl, p-methoxyphenyl, p-tolyl, benzyl or cyclohexyl group by reaction of methoxyacetone in an anhydrous ether with a Grignard reagent of formula RMgBr and hydrolysing the reaction mixture with a saturated aqueous solution of ammonium chloride to form a methoxypropanol of formula CH3CR(OH)CH2OCH3, heating this product in the absence of solvent with an acid sulphonic ion-exchange resin for 1 to 60 hours, and recovering the aldehyde by cooling and filtering off the resin. The products may be characterized by formation of their semicarbazones or 2,4-dinitrophenylhydrazones.
GB5161/65A 1962-03-10 1962-07-19 Improvements in or relating to ª‡-substituted propionaldehydes and process for theirproduction Expired GB1009916A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB5161/65A GB1009916A (en) 1962-03-10 1962-07-19 Improvements in or relating to ª‡-substituted propionaldehydes and process for theirproduction

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT473062 1962-03-10
GB5161/65A GB1009916A (en) 1962-03-10 1962-07-19 Improvements in or relating to ª‡-substituted propionaldehydes and process for theirproduction

Publications (1)

Publication Number Publication Date
GB1009916A true GB1009916A (en) 1965-11-17

Family

ID=41426310

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5161/65A Expired GB1009916A (en) 1962-03-10 1962-07-19 Improvements in or relating to ª‡-substituted propionaldehydes and process for theirproduction

Country Status (1)

Country Link
GB (1) GB1009916A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0092031A1 (en) * 1982-04-15 1983-10-26 Firmenich Sa 1(7)p-Menthene-9-al and its use as a perfuming and flavouring agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0092031A1 (en) * 1982-04-15 1983-10-26 Firmenich Sa 1(7)p-Menthene-9-al and its use as a perfuming and flavouring agent

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