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| 2-Bromo-3-methylbenzoic acid Basic information |
| 2-Bromo-3-methylbenzoic acid Chemical Properties |
Melting point | 135-138 °C (lit.) | Boiling point | 308.3±30.0 °C(Predicted) | density | 1.599±0.06 g/cm3(Predicted) | storage temp. | Sealed in dry,Room Temperature | solubility | soluble in Methanol | form | Powder | pka | 2.92±0.10(Predicted) | color | Off-white | CAS DataBase Reference | 53663-39-1(CAS DataBase Reference) |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 22-24/25-37-26 | WGK Germany | 3 | HazardClass | IRRITANT | HS Code | 29163990 |
| 2-Bromo-3-methylbenzoic acid Usage And Synthesis |
Chemical Properties | Off-white powder | Uses | 2-Bromo-3-methylbenzoic acid may be used to synthesize N-phenyl-3-methylanthranilic acid via copper-catalyzed amination reaction with aniline. | General Description | 2-Bromo-4-nitrotoluene is formed as an intermediate during the synthesis of 2-bromo-3-methylbenzoic acid. 2-Bromo-3-methylbenzoic acid can be obtained from 2-bromo-4-nitrotoluene via Von-Richter reaction. | Synthesis | The general procedure for synthesizing 2-bromo-3-methylbenzoic acid from 2-amino-3-methylbenzoic acid was as follows: referring to Example 1 (0142), 1.00 g of 2-amino-3-methylbenzoic acid, 8 mL of acetic acid, 4 mL of 50% hydrobromic acid, and 16 mL of water were mixed, followed by the addition of 0.46 g of sodium nitrite and 3 mL of water chilled on ice. After stirring the mixture in an ice bath for 10 minutes, the complete reaction of 2-amino-3-methylbenzoic acid was confirmed by silica gel thin layer chromatography (Spreader: hexane/ethyl acetate = 1/1, Rf value of 0.67 for 2-amino-3-methylbenzoic acid). Next, 1.42 g of copper bromide and 5 mL of water were added and the mixture was heated and reacted at 50 °C for 3 hours. Upon completion of the reaction, water was added to the mixture and the precipitate was collected by filtration to give 1.0 g of 2-bromo-3-methylbenzoic acid. (0143) 1H-NMR (CDCl3) δ (ppm): 2.49 (3H, s), 7.29 (1H, t, J=7.6Hz), 7.42 (1H, d, J=7.2Hz), 7.70 (1H, t, J=3.9Hz). | References | [1] Patent: US2017/57935, 2017, A1. Location in patent: Paragraph 0142; 0143 |
| 2-Bromo-3-methylbenzoic acid Preparation Products And Raw materials |
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