| Identification | Back Directory | [Name]
p-Nitrophenoxyamine | [CAS]
33543-55-4 | [Synonyms]
O-(4-Nitrophenyl) p-Nitrophenoxyamine O-(4-nitrophenyl)hydroxylaMine Hydroxylamine, O-(4-nitrophenyl)- | [EINECS(EC#)]
608-888-7 | [Molecular Formula]
C6H6N2O3 | [MDL Number]
MFCD12923172 | [MOL File]
33543-55-4.mol | [Molecular Weight]
154.12 |
| Chemical Properties | Back Directory | [Melting point ]
126-127℃ | [Boiling point ]
313.2±34.0 °C(Predicted) | [density ]
1.370±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C(protect from light) | [pka]
1.32±0.70(Predicted) | [Appearance]
White to yellow Solid |
| Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of O-(4-nitrophenyl)hydroxylamine from the compound (CAS: 83077-00-3) is as follows: wet ethyl N-(4-nitrophenoxy)acetimidate (781 g, dry wt.) was dissolved in 210 g of acetonitrile and the reaction temperature was adjusted to about 25 °C. Under the condition of keeping the reaction temperature below 30°C, 515 g of 37% hydrochloric acid was slowly added. The reaction mixture was stirred continuously at 25-30°C until the reaction was complete, which took about 2 hours. Subsequently, 209 g of 12% aqueous sodium hydroxide solution was slowly added to the reaction mixture at the same temperature range and stirring was continued for about 30 minutes. About 85% of the acetonitrile was removed by distillation at a jacket temperature of 50°C (internal temperature maintained at 25-30°C) under vacuum at 100 mbar. To the residue 20,900 g of water was added and the resulting slurry was stirred for 60 minutes. The product was collected by filtration, washed with 505 g of water and finally dried under vacuum at 40 °C. A final 560 g of O-(4-nitrophenyl)hydroxylamine was obtained in 94% yield. | [References]
[1] Patent: WO2010/38029, 2010, A1. Location in patent: Page/Page column 45 [2] Patent: WO2010/116140, 2010, A1. Location in patent: Page/Page column 47 [3] Patent: WO2009/44143, 2009, A2. Location in patent: Page/Page column 38 [4] Journal of Organic Chemistry, 1984, vol. 49, p. 1348 - 1352 [5] Journal of the American Chemical Society, 1982, vol. 104, # 23, p. 6393 - 6397 |
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