Identification | Back Directory | [Name]
3-BROMO-4-METHYL-5-NITROBENZOIC ACID | [CAS]
34545-20-5 | [Synonyms]
3-Bromo-4-methyl-5-nitro-benzoic Benzoic acid, 3-broMo-4-Methyl-5-nitro- | [Molecular Formula]
C8H6BrNO4 | [MDL Number]
MFCD02041260 | [MOL File]
34545-20-5.mol | [Molecular Weight]
260.04 |
Chemical Properties | Back Directory | [Boiling point ]
387.0±42.0 °C(Predicted) | [density ]
1.777±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
3.27±0.10(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
Step 3: 3-amino-4-methyl-5-nitrobenzoic acid (50 g, 254 mmol) was suspended in a mixture of concentrated hydrochloric acid (350 ml) and water (350 ml) at 0-5 °C. Subsequently, an aqueous solution of sodium nitrite (18.6 g, 270 mmol) (30 ml) was slowly added over 15 to 20 minutes. The reaction mixture was continued to be stirred at 0-5°C for 30 minutes. After that, the reaction mixture was slowly poured into a pre-cooled solution of concentrated hydrochloric acid (220 ml) of cuprous bromide (73.21 g, 516 mmol) and kept stirring at 0-5°C for 30 min followed by stirring at room temperature for 30 min. Finally, the reaction mixture was heated to 30-35 °C and stirred for 30 min, the precipitated solid was collected by filtration, washed with water (50 ml) and dried under vacuum to give 58 g of 3-bromo-4-methyl-5-nitrobenzoic acid as a pink solid in 88% yield.1H-NMR (CD3OD-d4) δppm: 2.6 (3H, s, CH3), 8.21 (1H, d , J = 1.4Hz, Ar-H), 8.27 (1H, d, J = 1.2Hz, Ar-H). | [References]
[1] Patent: WO2010/59549, 2010, A1. Location in patent: Page/Page column 16-17 [2] Justus Liebigs Annalen der Chemie, 1891, vol. 266, p. 223,227 |
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Anichem Inc.
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