N-Phenylhydroxylamine
Chemical compound
From Wikipedia, the free encyclopedia
N-Phenylhydroxylamine is the organic compound with the formula C6H5NHOH. It is an intermediate in the redox-related pair C6H5NH2 and C6H5NO. N-Phenylhydroxylamine should not be confused with its isomer α-phenylhydroxylamine or O-phenylhydroxylamine.
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| Names | |||
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| Preferred IUPAC name
N-Hydroxyaniline | |||
| Other names
beta-phenylhydroxylamine; phenylhydroxylamine; N-hydroxybenzeneamine; hydroxylaminobenzene | |||
| Identifiers | |||
3D model (JSmol) |
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| ECHA InfoCard | 100.002.614 | ||
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PubChem CID |
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| Properties | |||
| C6H7NO | |||
| Molar mass | 109.1274 g/mol | ||
| Appearance | yellow needles | ||
| Melting point | 80 to 81 °C (176 to 178 °F; 353 to 354 K) | ||
| â68.2·10â6 cm3/mol | |||
| Related compounds | |||
Related compounds |
hydroxylamine, nitrosobenzene | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Preparation
This compound can be prepared by the reduction of nitrobenzene with zinc in the presence of NH4Cl.[1][2]
Alternatively, it can be prepared by transfer hydrogenation of nitrobenzene using hydrazine as an H2 source over a rhodium catalyst.[3]
Reactions
Phenylhydroxylamine is unstable to heating, and in the presence of strong acids easily rearranges to 4-aminophenol via the Bamberger rearrangement. Oxidation of phenylhydroxylamine with dichromate gives nitrosobenzene.
Like other hydroxylamines it will react with aldehydes to form nitrones, illustrative is the condensation with benzaldehyde to form diphenylnitrone, a well-known 1,3-dipolar compound:[4]
- C6H5NHOH + C6H5CHO â C6H5N(O)=CHC6H5 + H2O
Phenylhydroxylamine is attacked by NO+ sources to give cupferron:[5]
- C6H5NHOH + C4H9ONO + NH3 â NH4[C6H5N(O)NO] + C4H9OH