ChemicalBook--->CAS DataBase List--->101580-70-5

101580-70-5

101580-70-5 Structure

101580-70-5 Structure
IdentificationBack Directory
[Name]

1,2-DibroMo-4-Methyl-5-nitrobenzene
[CAS]

101580-70-5
[Synonyms]

1,2-DibroMo-4-Methyl-5-nitrobenzene
Benzene, 1,2-dibromo-4-methyl-5-nitro-
[Molecular Formula]

C7H5Br2NO2
[MDL Number]

MFCD23135744
[MOL File]

101580-70-5.mol
[Molecular Weight]

294.93
Chemical PropertiesBack Directory
[Melting point ]

90.5-91.5 °C
[Boiling point ]

316.5±37.0 °C(Predicted)
[density ]

1.967±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

1,2-DibroMo-4-Methyl-5-nitrobenzene(101580-70-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

3,4-DIBROMOTOLUENE

60956-23-2

1,2-DibroMo-4-Methyl-5-nitrobenzene

101580-70-5

Step A: 3,4-dibromotoluene (108.11 mL, 800 mmol) was slowly added dropwise to 90% nitric acid (280 mL, 6000 mmol) pre-cooled to 0°C under nitrogen protection over a controlled period of 4 hours. The reaction mixture was mechanically stirred at 0°C to ensure that the internal temperature was always below 10°C. After the dropwise addition, stirring was continued at 0°C for 1 hour. Subsequently, water (840 mL) was added slowly, keeping the internal temperature below 10°C. The crude product was collected by filtration and washed thoroughly with water (5 x 500 mL) to remove residual nitric acid. The resulting solid was dried under high vacuum and then purified by recrystallization from ethanol (800 mL) to give 180.9 g (77% yield) of the target product 1,2-dibromo-4-methyl-5-nitrobenzene as a solid. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 8.24 (s, 1H), 7.64 (s, 1H), 2.55 (s, 3H).

[References]

[1] Patent: US2004/192653, 2004, A1
[2] Patent: US2006/264431, 2006, A1. Location in patent: Page/Page column 23
[3] Patent: WO2007/126871, 2007, A1. Location in patent: Page/Page column 65
[4] Chemische Berichte, 1881, vol. 14, p. 418
[5] Justus Liebigs Annalen der Chemie, 1873, vol. 168, p. 153
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