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Reaction of Lithiomethyl Isocyanide with Hexyl Bromide, Oxirane and Cyclohexanone

6 Reaction of Lithiomethyl Isocyanide with Hexyl Bromide, Oxirane, and Cyclohexanone (Note 1) [Pg.168]

In order to avoid complaints about the stench, all operations with isonitriles should be carried out in a well-ventilated hood. The glassware used for the syntheses can be cleaned with a mixture of acetone and dilute (4N) hydrochloric acid. [Pg.170]

If the temperature is allowed to rise too fast, the reaction mixture turns brown, due to (unknown) side-reactions, and yields of the products are considerably lower. [Pg.170]




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2-Hexyl bromide

2-Lithiomethyl

Bromide reaction

Cyclohexanone reaction

Cyclohexanones reactions with

Hexyl

Isocyanides reactions

Lithiomethyl isocyanide

Of cyclohexanone

Of cyclohexanones

Of oxiranes

Oxirane reactions

Oxiranes reactions

Reaction with bromides

Reaction with cyclohexanone

Reaction with isocyanides

Reaction with oxiranes

Reactions of isocyanides

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