(RS)-benzyl mandelate

Robila K. Mughal; Robin G. Pritchard; Roger J. Davey

doi:10.1107/S1600536804025024

(RS)-benzyl mandelate

Robila K. Mughal, Robin G. Pritchard, Roger J. Davey

Research output: Contribution to journal › Article › peer-review

Abstract

A benzyl ester of mandelic acid, C15H14O 3, was obtained by the crystallization of racemic mandelic acid from benzyl alcohol followed by vacuum drying at 363 K. The structure is composed of two hydrogen-bonded chains of S or R configuration, running along the shortest crystallographic b axis. There is one molecule in the asymmetric unit and each molecule forms four intermolecular hydrogen bonds with two other molecules of the same chirality. © 2004 International Union of Crystallography Printed in Great Britain - all rights reserved.

Original language	English
Pages (from-to)	o1984-o1986
Journal	Acta Crystallographica Section E: Structure Reports Online
Volume	60
Issue number	11
DOIs	https://doi.org/10.1107/S1600536804025024
Publication status	Published - Nov 2004

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10.1107/S1600536804025024

http://journals.iucr.org/e/issues/2004/11/00/wn6292/wn6292.pdf

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title = "(RS)-benzyl mandelate",

abstract = "A benzyl ester of mandelic acid, C15H14O 3, was obtained by the crystallization of racemic mandelic acid from benzyl alcohol followed by vacuum drying at 363 K. The structure is composed of two hydrogen-bonded chains of S or R configuration, running along the shortest crystallographic b axis. There is one molecule in the asymmetric unit and each molecule forms four intermolecular hydrogen bonds with two other molecules of the same chirality. {\textcopyright} 2004 International Union of Crystallography Printed in Great Britain - all rights reserved.",

author = "Mughal, {Robila K.} and Pritchard, {Robin G.} and Davey, {Roger J.}",

year = "2004",

month = nov,

doi = "10.1107/S1600536804025024",

language = "English",

volume = "60",

pages = "o1984--o1986",

journal = "Acta Crystallographica Section E: Structure Reports Online",

issn = "1600-5368",

publisher = "International Union of Crystallography",

number = "11",

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T1 - (RS)-benzyl mandelate

AU - Mughal, Robila K.

AU - Pritchard, Robin G.

AU - Davey, Roger J.

PY - 2004/11

Y1 - 2004/11

N2 - A benzyl ester of mandelic acid, C15H14O 3, was obtained by the crystallization of racemic mandelic acid from benzyl alcohol followed by vacuum drying at 363 K. The structure is composed of two hydrogen-bonded chains of S or R configuration, running along the shortest crystallographic b axis. There is one molecule in the asymmetric unit and each molecule forms four intermolecular hydrogen bonds with two other molecules of the same chirality. © 2004 International Union of Crystallography Printed in Great Britain - all rights reserved.

AB - A benzyl ester of mandelic acid, C15H14O 3, was obtained by the crystallization of racemic mandelic acid from benzyl alcohol followed by vacuum drying at 363 K. The structure is composed of two hydrogen-bonded chains of S or R configuration, running along the shortest crystallographic b axis. There is one molecule in the asymmetric unit and each molecule forms four intermolecular hydrogen bonds with two other molecules of the same chirality. © 2004 International Union of Crystallography Printed in Great Britain - all rights reserved.

U2 - 10.1107/S1600536804025024

DO - 10.1107/S1600536804025024

M3 - Article

SN - 1600-5368

VL - 60

SP - o1984-o1986

JO - Acta Crystallographica Section E: Structure Reports Online

JF - Acta Crystallographica Section E: Structure Reports Online

IS - 11

ER -

(RS)-benzyl mandelate

Abstract

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