4-Nitroaniline hydrochloride

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4-Nitroaniline hydrochloride Basic information
Product Name:4-Nitroaniline hydrochloride
Synonyms:P-NITRANILINE HYDROCHLORIDE;P-NITROANILINE HYDROCHLORIDE;1-AMINO-4-NITROBENZENE HYDROCHLORIDE;4-NITROPHENYLAMINE HYDROCHLORIDE;4-nitro-benzenaminmonohydrochloride;4-nitroanilinium chloride;1-Amino-4-nitrobenzeneHCl;Benzenamine, 4-nitro-, hydrochloride (1:1)
CAS:15873-51-5
MF:C6H7ClN2O2
MW:174.58
EINECS:239-997-4
Product Categories:Anilines, Aromatic Amines and Nitro Compounds
Mol File:15873-51-5.mol
4-Nitroaniline hydrochloride Structure
4-Nitroaniline hydrochloride Chemical Properties
Melting point 145-146 °C
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
color Light yellow to Amber to Dark green
EPA Substance Registry SystemBenzenamine, 4-nitro-, monohydrochloride (15873-51-5)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
TSCA TSCA listed
HS Code 2921.42.9000
MSDS Information
4-Nitroaniline hydrochloride Usage And Synthesis
Synthesis
1,4-DINITROBENZENE

100-25-4

4-NITROANILINE HYDROCHLORIDE

15873-51-5

GENERAL METHOD: To a 0.6 mL THF solution of the nitro compound (2 mmol) was added Fe(acac)3 (10 mol%, 70 mg) and TMDS (1.5 eq., equivalent to tris-Si-H, 0.53 mL). The reaction mixture was heated under constant stirring for 24 hours (unless otherwise stated). Upon completion of the reaction, the reaction mixture was diluted with a minimal amount of Et2O. Subsequently, a solution of Et2O with HCl (2 equivalents) was added dropwise. After precipitate generation was observed, stirring was continued for 5 minutes and then filtered. The precipitate was washed several times with Et2O and dried to give 4-nitroaniline hydrochloride.

References[1] Tetrahedron, 2011, vol. 67, # 10, p. 1971 - 1976
[2] Journal of Organic Chemistry, 2009, vol. 74, # 18, p. 6960 - 6964
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