Identification | Back Directory | [Name]
3-(2-AMINOETHYL)PYRIDINE | [CAS]
74317-85-4 | [Synonyms]
p-Anisicacid, 2-bromo- (6CI) Benzoicacid, 2-broMo-4-Methoxy- 2-Bromo-4-methoxybenzoic acid 98% 2-Bromo-p-anisic acid, 3-Bromo-4-carboxyanisole | [EINECS(EC#)]
214-589-6 | [Molecular Formula]
C8H7BrO3 | [MDL Number]
MFCD11044843 | [MOL File]
74317-85-4.mol | [Molecular Weight]
231.04 |
Chemical Properties | Back Directory | [Melting point ]
199℃ | [Boiling point ]
313.6±27.0 °C(Predicted) | [density ]
1.625±0.06 g/cm3 (20 ºC 760 Torr) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
solid | [pka]
3.12±0.10(Predicted) | [color ]
White to off-white |
Hazard Information | Back Directory | [Chemical Properties]
off-white powder | [Synthesis]
The general procedure for the synthesis of 2-bromo-4-methoxybenzoic acid from 4-methoxybenzoic acid was as follows: 152.3 g (1.0 mol) of 4-methoxybenzoic acid was added to a 2,000 mL four-necked flask fitted with a stirrer, a thermometer, and a reflux condenser tube, followed by the addition of 800 g of water and stirring until the 4-methoxybenzoic acid was completely dispersed. Then, 273.3 g (2.05 mol) of 30% aqueous sodium hydroxide was added. The temperature of the reaction solution was lowered to 0 °C and 167.8 g (1.05 mol) of bromine was slowly added dropwise over the temperature range of 0 to 5 °C. After the dropwise addition was completed, the reaction was continued with stirring for 1 hour by keeping the temperature at 0 to 5 °C. Upon completion of the reaction, 1.28 g (0.01 mol) of sodium sulfite was added to quench the reaction, followed by the addition of 100 g of toluene and raising the temperature of the reaction solution to 70 °C. The organic phase was removed by a liquid-liquid separation operation. To the aqueous phase obtained by separation 104.2 g (1.0 mol) of 35% hydrochloric acid was slowly added dropwise and stirred at room temperature for 1 hour. The precipitated solid product was collected by filtration and dried under reduced pressure to give 238.9 g (99.9% purity, 91.4% yield) of 2-bromo-4-methoxybenzoic acid. | [References]
[1] Patent: US2018/86687, 2018, A1. Location in patent: Paragraph 0064 |
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