Solid state acetylation with acetylimidazole: Selective protection of primary alcohols and phenols

Article abstract of DOI:10.1080/00397919808007174

Primary alcohols and phenols have been acetylated with acetylimidazole by the solid state reaction, grinding both substrates with a pestle in a mortar.

Full text of DOI:10.1080/00397919808007174

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Solid State Acetylation with
Acetylimidazole: Selective
Protection of Primary Alcohols
and Phenols
Hisahiro Hagiwara a , Kimie Morohashi a , Toshio
Suzuki a , Masayoshi Ando b , Isao Yamamoto c
Michiharu Kato c
&
a Graduate School of Science and Technology ,
Niigata University , 2-nocho, Ikarashi, Niigata,
950—21
b Faculty of Engineering , Niigata University , 2-
nocho, Ikarashi, Niigata, 950—21
c Institute for Chemical Reaction Science , Tohoku
University , Katahira, Aoba-ku, Sendai, 980—77,
JAPAN
Published online: 20 Aug 2006.
To cite this article: Hisahiro Hagiwara , Kimie Morohashi , Toshio Suzuki , Masayoshi
Ando , Isao Yamamoto & Michiharu Kato (1998) Solid State Acetylation with
Acetylimidazole: Selective Protection of Primary Alcohols and Phenols, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 28:11, 2001-2006, DOI: 10.1080/00397919808007174
To link to this article: http://dx.doi.org/10.1080/00397919808007174

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