ChemicalBook--->CAS DataBase List--->109466-84-4

109466-84-4

109466-84-4 Structure

109466-84-4 Structure
IdentificationBack Directory
[Name]

2-Amino-4-nitrobenzaldehyde
[CAS]

109466-84-4
[Synonyms]

2-Amino-4-nitrobenzaldehyde
Benzaldehyde, 2-amino-4-nitro-
[Molecular Formula]

C7H6N2O3
[MDL Number]

MFCD09264065
[MOL File]

109466-84-4.mol
[Molecular Weight]

166.13
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

Orange to red Solid
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-4-nitrobenzaldehyde(109466-84-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-AMINO-4-NITROBENZENEMETHANOL

78468-34-5

2-Amino-4-nitrobenzaldehyde

109466-84-4

GENERAL STEPS: (2-Amino-4-nitrophenyl)methanol (650 mg, 3.87 mmol) was reacted with manganese dioxide (1680 mg, 19.33 mmol) in a solvent mixture of tetrahydrofuran (5 mL) and dichloromethane (25 mL) with stirring for 2 hours at room temperature. Upon completion of the reaction, the reaction mixture was filtered to remove insoluble solids and the filtrate was subsequently concentrated. The resulting crude product was purified by silica gel column chromatography (eluent: 40%-50% hexane solution of ethyl acetate; silica gel column: 25 g) to afford the target compound 2-amino-4-nitrobenzaldehyde (550 mg, 86% yield) as an orange solid. Its 1H NMR (400 MHz, DMSO-d6) data were as follows: δ 9.99 (s, 1H), 7.85 (d, J = 8.6 Hz, 1H), 7.63 (d, J = 2.3 Hz, 1H), 7.55 (br.s., 2H), 7.35 (dd, J = 8.6, 2.3 Hz, 1H).

[References]

[1] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 19, p. 5810 - 5831
[2] Patent: WO2015/6100, 2015, A1. Location in patent: Page/Page column 113
[3] Patent: EP2128157, 2009, A1. Location in patent: Page/Page column 103
[4] Patent: WO2015/95795, 2015, A1. Location in patent: Paragraph 0586
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