Abstract:The synthesis of 1,4-diisocyanato-4-methylpentane was accomplished starting from isobutyronitrile in six steps with 53% overall yield. The two isocyanates were installed by a double Curtius rearrangement. The product reacts with alcohol in a regioselective manner.
Diisocyanate (VIII) is regioselectively synthesized starting from isobutyronitrile in six steps using a double Curtius rearrangement as the key reaction.
Diisocyanate (VIII) is regioselectively synthesized starting from isobutyronitrile in six steps using a double Curtius rearrangement as the key reaction.
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