ES8207504A1 - Manufacture of aromatic compound - Google Patents

Manufacture of aromatic compound

Info

Publication number
ES8207504A1
ES8207504A1 ES501670A ES501670A ES8207504A1 ES 8207504 A1 ES8207504 A1 ES 8207504A1 ES 501670 A ES501670 A ES 501670A ES 501670 A ES501670 A ES 501670A ES 8207504 A1 ES8207504 A1 ES 8207504A1
Authority
ES
Spain
Prior art keywords
salt
transformed
group
compound
manufacture
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
ES501670A
Other languages
Spanish (es)
Other versions
ES501670A0 (en
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.)
Novartis AG
Original Assignee
Ciba Geigy AG
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 Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of ES501670A0 publication Critical patent/ES501670A0/en
Publication of ES8207504A1 publication Critical patent/ES8207504A1/en
Expired legal-status Critical Current

Links

Landscapes

  • Hydrogenated Pyridines (AREA)
  • Epoxy Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Procedure for the obtaining of 1-2 (-alylloxylenoxy) -3-isopropyl-amino-2-propanol. Consists of transforming, in a compound (I), or in a salt thereof, the epoxipropiloxi group in the aliloxi group by action of diffosforic tetrahydride, in the sine of a solvent, such as the ether dirty, at a temperature comprised between 20 and 60 centigred degrees. If desired, the free compound obtained is transformed into a salt or a salt obtained is transformed in the free compound. The compound obtained has the formula (III). The transformation has place preferably in the presence of an organic nitrogen base, such as trietilamine, N-etilpipe-ridine, pyridine, cholidine or quinoline. (Machine-translation by Google Translate, not legally binding)
ES501670A 1980-04-29 1981-04-27 Manufacture of aromatic compound Expired ES8207504A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH330180 1980-04-29

Publications (2)

Publication Number Publication Date
ES501670A0 ES501670A0 (en) 1982-09-16
ES8207504A1 true ES8207504A1 (en) 1982-09-16

Family

ID=4253023

Family Applications (1)

Application Number Title Priority Date Filing Date
ES501670A Expired ES8207504A1 (en) 1980-04-29 1981-04-27 Manufacture of aromatic compound

Country Status (4)

Country Link
JP (1) JPS56169654A (en)
AT (1) AT375065B (en)
ES (1) ES8207504A1 (en)
FI (1) FI811284L (en)

Also Published As

Publication number Publication date
ES501670A0 (en) 1982-09-16
JPS56169654A (en) 1981-12-26
FI811284L (en) 1981-10-30
AT375065B (en) 1984-06-25
ATA190381A (en) 1983-11-15

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