ChemicalBook--->CAS DataBase List--->74317-85-4

74317-85-4

74317-85-4 Structure

74317-85-4 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P280
[HS Code ]

2918999090
Hazard InformationBack Directory
[Chemical Properties]

off-white powder
[Synthesis]

4-Methoxybenzoic acid

100-09-4

3-(2-AMINOETHYL)PYRIDINE

74317-85-4

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
Spectrum DetailBack Directory
[Spectrum Detail]

3-(2-AMINOETHYL)PYRIDINE(74317-85-4)1HNMR
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