1963
DOI: 10.1002/prac.19630200103
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Synthese potentieller Cytostatica. II. 4,4′‐Dibrom‐dialkyläther mit sekundären Brom‐ oder Äthergruppen

Abstract: 3,3′‐Dibrom‐dipropyläther wurde unter Verwendung von Tetrahydrofuran als Lösungsmittel in die entsprechende bifunktionelle Grignard‐Verbindung überführt, diese mit aliphatischen Aldehyden oder Aceton zu 4,4′‐Dihydroxy‐dialkyläthern umgesetzt und daraus die Bromäther hergestellt. Außerdem wurden Bis‐(4‐brombutoxy)‐octan‐(2,7) und 3,3′,4,4′,‐Tetrabrom‐dibutyläther Synthetisiert.

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Cited by 11 publications
(2 citation statements)
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“…[26] The thiol group was obtained using the Bunte salt method. [27±29] (2-Hydroxy-ethyl)-phenylethyl-ether (a): A mixture of sodium (8 g) and phenyl ethanol (100 g) were heated up to 70 8C.…”
Section: Methodsmentioning
confidence: 99%
“…[26] The thiol group was obtained using the Bunte salt method. [27±29] (2-Hydroxy-ethyl)-phenylethyl-ether (a): A mixture of sodium (8 g) and phenyl ethanol (100 g) were heated up to 70 8C.…”
Section: Methodsmentioning
confidence: 99%
“…The conversion of 14 to 17 has previously been accomplished in 57% yield. 22 We have improved this by proceeding through the intermediate23 15, which was added to a solution formed by treating sodium with excess 1,3-propanediol to form 16. Hydrolysis of 16 yielded 17 in 70% overall yield from 14. The remaining steps were carried out essentially as in the syntheses of 4 and 5.…”
mentioning
confidence: 99%