GR21272B - METHOD OF PREPARATION OF PIPERIDINE PRODUCERS. - Google Patents

METHOD OF PREPARATION OF PIPERIDINE PRODUCERS.

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Publication number
GR21272B
GR21272B GR600121272A GR600121272A GR21272B GR 21272 B GR21272 B GR 21272B GR 600121272 A GR600121272 A GR 600121272A GR 600121272 A GR600121272 A GR 600121272A GR 21272 B GR21272 B GR 21272B
Authority
GR
Greece
Prior art keywords
degrees celsius
organic acid
preparation
propin
radical
Prior art date
Application number
GR600121272A
Other languages
Greek (el)
Original Assignee
Societe Des Laboratoires Labaz
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 Societe Des Laboratoires Labaz filed Critical Societe Des Laboratoires Labaz
Priority to GR600121272A priority Critical patent/GR21272B/en
Publication of GR21272B publication Critical patent/GR21272B/en

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Abstract

έθοδος παρασκευής αλάτων των εστέρων της (προπιν-2'-υλο-1')-4-πιπεριδινόλης -(4) αντιστοιχούντων είς τον γενικόν τύπον (Ι) εις τον οποίον το R παριστά ευθείαν μονοσθενή άλυσιν αλειφατικής υδρογονανθρακικής ρίζης από C1 έως C4, αλκοξυαλκυλομάδα, φαινοξυαλκυλομάδα κυκλοαλειφατικήν ή ευθείαν ή διακεκλαδισμένην αλκυλαρωματικήν ρίζαν, το R1 παριστά ρίζαν οργανικού οξέος και το ΗΧ οργανικό ή ανόργανονοξύ. Είς την μέθοδον ταύτην αντιδρά έν προπιν-2-υλο-1 αλίδιον, παρουσία μαγνησίου, αργιλλιου ή ψευδαργύρου και αιθήρ τις, είς θερμοκρασίαν μεταξύ -10βαθμούς κελσίου και 50 βαθμούς κελσίου, μετά μιάςΝ-υποκατεστημένης πιπεριδόνης. Το ούτω ληφθέν μεταλλικόν σύμπλοκον δύναται να υδρολυθή και ακολούθως να εστεροποιηθή, ή να εστεροποιηθή απ' ευθείας,είς θερμοκρασίαν 15 βαθμούς κελσίου έως 65 βαθμούς κελσίου, τη βοηθεία ανυδρίτου οργανικού οξέος, καιούτω ο ληφθείς βαικός εσθήρ μετατρέπεται τη βοηθεία οργανικού ή ανοργάνου οξέος είς το αντίστοιχον άλας. process for the preparation of salts of the esters of (propin-2'-yl-1 ') - 4-piperidinol - (4) corresponding to general formula (I) wherein R represents a straight monovalent chain of an aliphatic hydrocarbon radical from C1 to C4, alkoxyalkyl group, phenoxyalkyl group cycloaliphatic or straight or branched alkyl aromatic radical, R1 represents organic acid radical and HX represents organic or inorganic acid. The process is reacted with a propin-2-yl-1 allion in the presence of magnesium, aluminum or zinc and ethers at temperatures between -10 degrees Celsius and 50 degrees Celsius, followed by an N-substituted piperidone. The metal complex thus obtained can be hydrolyzed and then esterified, or esterified directly, at a temperature of 15 degrees Celsius to 65 degrees Celsius, with the help of anhydrous organic acid, so that the obtained organic acid is corresponding salt.

GR600121272A 1960-08-06 1960-08-06 METHOD OF PREPARATION OF PIPERIDINE PRODUCERS. GR21272B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GR600121272A GR21272B (en) 1960-08-06 1960-08-06 METHOD OF PREPARATION OF PIPERIDINE PRODUCERS.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GR600121272A GR21272B (en) 1960-08-06 1960-08-06 METHOD OF PREPARATION OF PIPERIDINE PRODUCERS.

Publications (1)

Publication Number Publication Date
GR21272B true GR21272B (en) 1960-10-12

Family

ID=36862290

Family Applications (1)

Application Number Title Priority Date Filing Date
GR600121272A GR21272B (en) 1960-08-06 1960-08-06 METHOD OF PREPARATION OF PIPERIDINE PRODUCERS.

Country Status (1)

Country Link
GR (1) GR21272B (en)

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