Identification | Back Directory | [Name]
4-(1H-PYRROL-1-YL)ANILINE | [CAS]
52768-17-9 | [Synonyms]
ASISCHEM A93505 BUTTPARK 98\12-84 4-(1-Pyrrolyl)aniline 4-Pyrrol-1-yl-aniline 1-(4-AMINOPHENYL)PYRROLE 4-(1H-PYRROL-1-YL)ANILINE 4-Pyrrol-1-yl-phenylamine Benzenamine, 4-(1H-pyrrol-1-yl)- | [Molecular Formula]
C10H10N2 | [MDL Number]
MFCD01934575 | [MOL File]
52768-17-9.mol | [Molecular Weight]
158.2 |
Chemical Properties | Back Directory | [Melting point ]
81 °C | [Boiling point ]
307.8±25.0 °C(Predicted) | [density ]
1.09±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [pka]
3.36±0.10(Predicted) | [Appearance]
Off-white to light yellow Solid |
Hazard Information | Back Directory | [Synthesis]
Under standard reaction conditions, 5.0 mg of Pd-gCN catalyst (containing 5.0 wt% Pd) was added to an ethanol solution (2 mL) containing 1.0 mM 1-(4-nitrophenyl)-1H-pyrrole, followed by the addition of 2 mM (1.2 eq., 0.07 mL) of 60% hydrazine hydrate solution. The reaction mixture was transferred to a 10 mL round bottom flask and reacted at reflux temperature (70 °C) for 4 hours. After completion of the reaction, the mixture was cooled to room temperature and the catalyst was isolated by filtration. The filtrate was purified by silica gel column chromatography to give 4-(1-pyrrolyl)aniline. For dinitroaromatic substrates, 4.0 mM (2.4 eq., 0.14 mL) of 60% hydrazine hydrate solution is required. | [References]
[1] Applied Catalysis A: General, 2016, vol. 523, p. 31 - 38 [2] European Journal of Medicinal Chemistry, 2015, vol. 96, p. 369 - 380 [3] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 1996, vol. 51, # 6, p. 757 - 764 [4] Recueil des Travaux Chimiques des Pays-Bas, 1943, vol. 62, p. 177,181, 183 [5] Farmaco, Edizione Scientifica, 1983, vol. 38, # 4, p. 219 - 231 |
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