ChemicalBook--->CAS DataBase List--->7149-14-6

7149-14-6

7149-14-6 Structure

7149-14-6 Structure
IdentificationBack Directory
[Name]

2-Bromo-1-iodo-4-nitrobenzene
[CAS]

7149-14-6
[Synonyms]

2-Bromo-1-iodo-4-nitrobenzene
Benzene, 2-bromo-1-iodo-4-nitro-
[Molecular Formula]

C6H3BrINO2
[MDL Number]

MFCD09878135
[MOL File]

7149-14-6.mol
[Molecular Weight]

327.9
Chemical PropertiesBack Directory
[Melting point ]

106 °C(Solv: ethyl acetate (141-78-6))
[Boiling point ]

332.7±27.0 °C(Predicted)
[density ]

2.349±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C, protect from light
[Appearance]

Light yellow to orange Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
[HS Code ]

2904990090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Bromo-1-iodo-4-nitrobenzene(7149-14-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-BROMO-4-NITROANILINE

13296-94-1

2-Bromo-1-iodo-4-nitrobenzene

7149-14-6

The general procedure for the synthesis of 3-bromo-4-iodonitrobenzene from 2-bromo-4-nitroaniline is as follows: a pre-cooled solution of sodium nitrite (57.2 g, 829 mmol) and potassium iodide (138 g, 829 mmol) dissolved in water (25 mL) was added dropwise to a stirred 2-bromo-4-nitroaniline (60 g 276 mmol) in acetonitrile (250 mL) suspension. After the dropwise addition was completed, the reaction mixture was continued to be stirred at 0-5 °C for 30 min. Upon completion of the reaction, the reaction mixture was slowly poured into pre-cooled water (1000 mL). The precipitated solid product was collected by filtration, washed with water several times and then dried to give the target compound 3-bromo-4-iodonitrobenzene. Yield: 70.0 g in 77% yield. The product characterization data were as follows: 1H NMR (300 MHz, CDCl3): δ 7.86 (dd, 1H, J = 8.7, 2.4 Hz, Ar-H), 8.10 (d, 1H, J = 8.7 Hz, Ar-H), 8.45 (d, 1H, J = 2.4 Hz, Ar-H); MS (EI, 70 eV): m/z 328.3 (M + H).

[References]

[1] Patent: WO2015/49629, 2015, A1. Location in patent: Page/Page column 102
[2] Gazzetta Chimica Italiana, 1874, vol. 4, p. 341
[3] Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften, 1875, p. 317
[4] Chemistry - A European Journal, 2017, vol. 23, # 11, p. 2660 - 2665
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