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  Home > JCE Print > Journal of Chemical Education > Issues > 1999  > September  >
In the Laboratory
The Microscale Laboratory
Microscale Synthesis of Tributyl Arsenite
Francisco J. Arnáiz and Mariano J. Miranda
Universidad de Burgos, Laboratorio de Química Inorgánica, 09001 Burgos, Spain

Cover
September 1999
Vol. 76 No. 9
p. 1251

Abstract
The most common ways to prepare arsenite esters make use of the reaction of arsenic trichloride with either sodium alkoxides, or alcohols in the presence of tertiary amines. Arsenic trichloride is a moisture-sensitive product for which the recently reported synthesis - direct reaction of arsenic(III) oxide with excess thionyl chloride - is not as simple as it appears, because the excess thionyl chloride is difficult to remove. Here we describe a simple synthesis for tributyl arsenite that makes use of the reaction of arsenic(III) oxide with butanol.
More Information
*  Citation
Arn‡iz, Francisco J.; Miranda, Mariano J. J. Chem. Educ. 1999 76 1251.
*  Keywords
Inorganic Chemistry; Arsenic; Synthesis; Microscale; Inorganic Synthesis
*  History
Created:
Last Updated:
July 30, 1999
June 23, 2005
  Home > JCE Print > Journal of Chemical Education > Issues > 1999 > September > Page 1251


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