HIGHLY SELECTIVE REDUCING AGENTS. REDUCTION OF NITROBENZENE TO ANILINE IN THE PRESENCE OF ALDEHYDES, ALKYL HALIDES, AND ACID HALIDES.

DOI: 10.1016/S0040-4039(00)80685-1

Source and publish data:

Tetrahedron Letters p. 5083 - 5086 (1988)

Update date:2022-08-12

Topics:

Authors:

Gaus, P.L.

Gerritz, Samuel W.

Jeffries, Patrick M.

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Article abstract of DOI:10.1016/S0040-4039(00)80685-1

Although the anionic hydride ^- is capable of reducing ketones and aldehydes under acidic conditions, it also selectively reduces nitrobenzene to aniline, even in the presence of benzaldehyde, benzyl chloride, or benzoyl chloride.

Full text of DOI:10.1016/S0040-4039(00)80685-1

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