Homogeneous hydroxyethylation of phenyl-substituted alcohols

Péter Sallay, Mohamed H M Ahmed, István Rusznák, László Farkas, A. Tungler

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Homogeneous glycol ether derivatives of phenyl group substituted alcohols (benzyl-, β-phenyl ethyl- and γ-phenyl propyl-) were synthesised by repeated Williamson synthesis starting in two cases from the halogen derivatives of the corresponding alcohols. In the case of β-phenylethanol the first homologue was prepared in the reaction of benzyl group protected ethylene chlorohydrine and β-phenyl-ethyl alcohol. The reaction product was hydrogenolysed (removing the benzyl group by hydrogenolyzis), halogenated and used to the synthesis of higher homologues as starting material.

Original languageEnglish
Pages (from-to)21-26
Number of pages6
JournalACH - Models in Chemistry
Volume133
Issue number1-2
Publication statusPublished - 1996

Fingerprint

Benzyl Alcohols
Alcohols
Phenylethyl Alcohol
Derivatives
Halogens
Glycols
Reaction products
Ether
Ethanol
ethylene

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Sallay, P., Ahmed, M. H. M., Rusznák, I., Farkas, L., & Tungler, A. (1996). Homogeneous hydroxyethylation of phenyl-substituted alcohols. ACH - Models in Chemistry, 133(1-2), 21-26.

Homogeneous hydroxyethylation of phenyl-substituted alcohols. / Sallay, Péter; Ahmed, Mohamed H M; Rusznák, István; Farkas, László; Tungler, A.

In: ACH - Models in Chemistry, Vol. 133, No. 1-2, 1996, p. 21-26.

Research output: Contribution to journalArticle

Sallay, P, Ahmed, MHM, Rusznák, I, Farkas, L & Tungler, A 1996, 'Homogeneous hydroxyethylation of phenyl-substituted alcohols', ACH - Models in Chemistry, vol. 133, no. 1-2, pp. 21-26.
Sallay P, Ahmed MHM, Rusznák I, Farkas L, Tungler A. Homogeneous hydroxyethylation of phenyl-substituted alcohols. ACH - Models in Chemistry. 1996;133(1-2):21-26.
Sallay, Péter ; Ahmed, Mohamed H M ; Rusznák, István ; Farkas, László ; Tungler, A. / Homogeneous hydroxyethylation of phenyl-substituted alcohols. In: ACH - Models in Chemistry. 1996 ; Vol. 133, No. 1-2. pp. 21-26.
@article{fe6f34708f364e03b0fef44b0e8a0c7d,
title = "Homogeneous hydroxyethylation of phenyl-substituted alcohols",
abstract = "Homogeneous glycol ether derivatives of phenyl group substituted alcohols (benzyl-, β-phenyl ethyl- and γ-phenyl propyl-) were synthesised by repeated Williamson synthesis starting in two cases from the halogen derivatives of the corresponding alcohols. In the case of β-phenylethanol the first homologue was prepared in the reaction of benzyl group protected ethylene chlorohydrine and β-phenyl-ethyl alcohol. The reaction product was hydrogenolysed (removing the benzyl group by hydrogenolyzis), halogenated and used to the synthesis of higher homologues as starting material.",
author = "P{\'e}ter Sallay and Ahmed, {Mohamed H M} and Istv{\'a}n Ruszn{\'a}k and L{\'a}szl{\'o} Farkas and A. Tungler",
year = "1996",
language = "English",
volume = "133",
pages = "21--26",
journal = "ACH - Models in Chemistry",
issn = "1217-8969",
publisher = "Akademiai Kiado",
number = "1-2",

}

TY - JOUR

T1 - Homogeneous hydroxyethylation of phenyl-substituted alcohols

AU - Sallay, Péter

AU - Ahmed, Mohamed H M

AU - Rusznák, István

AU - Farkas, László

AU - Tungler, A.

PY - 1996

Y1 - 1996

N2 - Homogeneous glycol ether derivatives of phenyl group substituted alcohols (benzyl-, β-phenyl ethyl- and γ-phenyl propyl-) were synthesised by repeated Williamson synthesis starting in two cases from the halogen derivatives of the corresponding alcohols. In the case of β-phenylethanol the first homologue was prepared in the reaction of benzyl group protected ethylene chlorohydrine and β-phenyl-ethyl alcohol. The reaction product was hydrogenolysed (removing the benzyl group by hydrogenolyzis), halogenated and used to the synthesis of higher homologues as starting material.

AB - Homogeneous glycol ether derivatives of phenyl group substituted alcohols (benzyl-, β-phenyl ethyl- and γ-phenyl propyl-) were synthesised by repeated Williamson synthesis starting in two cases from the halogen derivatives of the corresponding alcohols. In the case of β-phenylethanol the first homologue was prepared in the reaction of benzyl group protected ethylene chlorohydrine and β-phenyl-ethyl alcohol. The reaction product was hydrogenolysed (removing the benzyl group by hydrogenolyzis), halogenated and used to the synthesis of higher homologues as starting material.

UR - http://www.scopus.com/inward/record.url?scp=0002154793&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0002154793&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0002154793

VL - 133

SP - 21

EP - 26

JO - ACH - Models in Chemistry

JF - ACH - Models in Chemistry

SN - 1217-8969

IS - 1-2

ER -