Nitrogen dioxide - Sodium iodide as an efficient reagent for the one- pot conversion of aryl amines to aryl iodides under nonaqueous conditions

DOI: 10.1016/S0040-4039(98)00824-7

Source and publish data:

Tetrahedron Letters p. 4533 - 4536 (1998)

Update date:2022-08-11

Topics:

Authors:

Suzuki, Hitomi

Nonoyama, Nobuaki

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Article abstract of DOI:10.1016/S0040-4039(98)00824-7

Successive treatment of aromatic amines with liquid nitrogen dioxide and powdered sodium iodide in acetonitrile at -20 °C, followed by usual work- up, gave the corresponding aryl iodides in good yield. This method worked especially well for less basic amines bearing electron-withdrawing substituents.

Full text of DOI:10.1016/S0040-4039(98)00824-7

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