Catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin

Two new and improved procedures were developed for the synthesis of 1-(1-naphthyloxy)-2,3-epoxypropane as an important intermediate in the production of the beta-blocker and antioxidant 1-[(1-methylethyl)amino]-3-(1-naphthyloxy)- 2-propanol (propranolol). Both base homogeneous and heterogeneous PTC...

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Main Authors: Jovanović Slobodanka, Vico-Stevanović Milanka, Uglješić-Kilibarda Dragana, Popadić Dragica, Simić Slobodanka, Dželetović Dijamanda
Format: Article
Language:English
Published: Serbian Chemical Society 2006-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0352-5139/2006/0352-51390609867J.pdf
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spelling doaj-bcbfaf4f346740e6ae814a10435a82272020-12-24T14:30:55ZengSerbian Chemical Society Journal of the Serbian Chemical Society0352-51391820-74212006-01-01718-986787710.2298/JSC0609867J0352-51390609867JCatalysis in the alkylation reaction of 1-naphthol with epichlorohydrinJovanović Slobodanka0Vico-Stevanović Milanka1Uglješić-Kilibarda Dragana2Popadić Dragica3Simić Slobodanka4Dželetović Dijamanda5Galenika a.d., BeogradGalenika a.d., BeogradGalenika a.d., BeogradGalenika a.d., BeogradGalenika a.d., BeogradGalenika a.d., BeogradTwo new and improved procedures were developed for the synthesis of 1-(1-naphthyloxy)-2,3-epoxypropane as an important intermediate in the production of the beta-blocker and antioxidant 1-[(1-methylethyl)amino]-3-(1-naphthyloxy)- 2-propanol (propranolol). Both base homogeneous and heterogeneous PTC catalysis were employed. High yields and remarkable selectivity were achieved. The improved purity is particularly important, in view of the quality requirements for propranolol hydrochloride as an active pharmaceutical ingredient.http://www.doiserbia.nb.rs/img/doi/0352-5139/2006/0352-51390609867J.pdfheterogeneous ptc catalysisbase homogeneous catalysisselectivityyieldmodel system
collection DOAJ
language English
format Article
sources DOAJ
author Jovanović Slobodanka
Vico-Stevanović Milanka
Uglješić-Kilibarda Dragana
Popadić Dragica
Simić Slobodanka
Dželetović Dijamanda
spellingShingle Jovanović Slobodanka
Vico-Stevanović Milanka
Uglješić-Kilibarda Dragana
Popadić Dragica
Simić Slobodanka
Dželetović Dijamanda
Catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin
Journal of the Serbian Chemical Society
heterogeneous ptc catalysis
base homogeneous catalysis
selectivity
yield
model system
author_facet Jovanović Slobodanka
Vico-Stevanović Milanka
Uglješić-Kilibarda Dragana
Popadić Dragica
Simić Slobodanka
Dželetović Dijamanda
author_sort Jovanović Slobodanka
title Catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin
title_short Catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin
title_full Catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin
title_fullStr Catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin
title_full_unstemmed Catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin
title_sort catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin
publisher Serbian Chemical Society
series Journal of the Serbian Chemical Society
issn 0352-5139
1820-7421
publishDate 2006-01-01
description Two new and improved procedures were developed for the synthesis of 1-(1-naphthyloxy)-2,3-epoxypropane as an important intermediate in the production of the beta-blocker and antioxidant 1-[(1-methylethyl)amino]-3-(1-naphthyloxy)- 2-propanol (propranolol). Both base homogeneous and heterogeneous PTC catalysis were employed. High yields and remarkable selectivity were achieved. The improved purity is particularly important, in view of the quality requirements for propranolol hydrochloride as an active pharmaceutical ingredient.
topic heterogeneous ptc catalysis
base homogeneous catalysis
selectivity
yield
model system
url http://www.doiserbia.nb.rs/img/doi/0352-5139/2006/0352-51390609867J.pdf
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AT ugljesickilibardadragana catalysisinthealkylationreactionof1naphtholwithepichlorohydrin
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