Journal of Japan Oil Chemists' Society
Online ISSN : 1884-2003
ISSN-L : 0513-398X
Reaction of Styrene Oxide in the Presence of Ion-exchange Resins
Takeo KURATANobuyuki KOBAYASHI
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JOURNAL FREE ACCESS

1989 Volume 38 Issue 1 Pages 82-87

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Abstract
The reactions of styrene oxide (1) with acetone, the isomerization of oxides, and reactions of (1) with alcohols in the presence of H-form ion-exchange resins (Dowex 50W-X8, Dowex 50 W-X4, Diaion PK 216, Amberlyst 15 and Nafion NR 50) were studied.
The following results were obtained : 2, 2-Dimethyl-4-phenyl-1, 3-dioxolane was synthesized in a high yield (isolated yield 93%) by a simple reaction of (1) with acetone catalyzed by Amberlyst 15 or Nafion NR 50.
Phenylacetaldehyde was obtained (isolated yield 91%) by the isomerization of (1) catalyzed by Amberlyst 15 or Nafion NR 50.
2-Phenyl-2-methoxyethanol was obtained in a high yield by the reaction of (1) with methanol catalyzed by ion-exchange resins.
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