Syntheses of 2-(2-Quinoxalyl)-1-Phenylethanone and Related Ethanones

Eldon H. Sund; David L. Callender

doi:10.1021/je60085a004

Syntheses of 2-(2-Quinoxalyl)-1-Phenylethanone and Related Ethanones

Eldon H. Sund, David L. Callender

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

1 Scopus citations

Abstract

Nine 2-(2-quinoxalyl)-1-phenylethanones were synthesized by the condensation of 2-methylquinoxaline and the requisite methyl benzoate ester with sodium hydride as the condensing agent. Substituents in the 3 or 4 positions of the phenyl ring were methyl, methoxy, chloro, or trifluoromethyl.

Original language	English (US)
Pages (from-to)	189
Number of pages	1
Journal	Journal of Chemical and Engineering Data
Volume	25
Issue number	2
DOIs	https://doi.org/10.1021/je60085a004
State	Published - Apr 1 1980
Externally published	Yes

ASJC Scopus subject areas

General Chemistry
General Chemical Engineering

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title = "Syntheses of 2-(2-Quinoxalyl)-1-Phenylethanone and Related Ethanones",

abstract = "Nine 2-(2-quinoxalyl)-1-phenylethanones were synthesized by the condensation of 2-methylquinoxaline and the requisite methyl benzoate ester with sodium hydride as the condensing agent. Substituents in the 3 or 4 positions of the phenyl ring were methyl, methoxy, chloro, or trifluoromethyl.",

author = "Sund, \{Eldon H.\} and Callender, \{David L.\}",

year = "1980",

month = apr,

day = "1",

doi = "10.1021/je60085a004",

language = "English (US)",

volume = "25",

pages = "189",

journal = "Journal of Chemical and Engineering Data",

issn = "0021-9568",

publisher = "American Chemical Society",

number = "2",

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T1 - Syntheses of 2-(2-Quinoxalyl)-1-Phenylethanone and Related Ethanones

AU - Sund, Eldon H.

AU - Callender, David L.

PY - 1980/4/1

Y1 - 1980/4/1

N2 - Nine 2-(2-quinoxalyl)-1-phenylethanones were synthesized by the condensation of 2-methylquinoxaline and the requisite methyl benzoate ester with sodium hydride as the condensing agent. Substituents in the 3 or 4 positions of the phenyl ring were methyl, methoxy, chloro, or trifluoromethyl.

AB - Nine 2-(2-quinoxalyl)-1-phenylethanones were synthesized by the condensation of 2-methylquinoxaline and the requisite methyl benzoate ester with sodium hydride as the condensing agent. Substituents in the 3 or 4 positions of the phenyl ring were methyl, methoxy, chloro, or trifluoromethyl.

UR - https://www.scopus.com/pages/publications/33847086044

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U2 - 10.1021/je60085a004

DO - 10.1021/je60085a004

M3 - Article

AN - SCOPUS:33847086044

SN - 0021-9568

VL - 25

SP - 189

JO - Journal of Chemical and Engineering Data

JF - Journal of Chemical and Engineering Data

IS - 2

ER -

Syntheses of 2-(2-Quinoxalyl)-1-Phenylethanone and Related Ethanones

Abstract

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