| Identification | Back Directory | [Name]
BENZOIC ACID, 4-AMINO-2-BROMO-, METHYL ESTER | [CAS]
98545-64-3 | [Synonyms]
Methyl 4-aMino-2-broMobenzoate
methyl-2-bromo-4-aminobenzoate
4-AMINO-2-BROMO-BENZOIC ACID METHYL ESTER
BENZOIC ACID, 4-AMINO-2-BROMO-, METHYL ESTER | [Molecular Formula]
C8H8BrNO2 | [MDL Number]
MFCD00859376 | [MOL File]
98545-64-3.mol | [Molecular Weight]
230.06 |
| Chemical Properties | Back Directory | [Melting point ]
94 °C | [Boiling point ]
345.2±22.0 °C(Predicted) | [density ]
1.578±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [pka]
1.39±0.10(Predicted) | [Appearance]
Light yellow to light brown Solid |
| Hazard Information | Back Directory | [Uses]
Methyl 4-amino-2-bromobenzoate is an organic compound that is commonly used as a synthetic intermediate, especially in the pharmaceutical industry, for the synthesis of biologically active compounds. | [Synthesis]
General procedure for the synthesis of methyl 4-amino-2-bromobenzoate from methyl 2-bromo-4-nitrobenzoate: To a solution of methyl 2-bromo-4-nitrobenzoate (4.5 g, 17.0 mmol) in ethyl acetate (100 mL) was added stannous chloride dihydrate (38.3 g, 0.17 mol). The reaction mixture was heated to reflux and stirred for 4 hours. Upon completion of the reaction, the mixture was poured into a mixture of saturated sodium bicarbonate solution (500 mL) and ethyl acetate (370 mL). The organic layer was separated, washed with saturated brine (300 mL) and dried with anhydrous magnesium sulfate. After concentration under reduced pressure, the residue was purified by silica gel column chromatography to afford methyl 4-amino-2-bromobenzoate as a solid (3.68 g, 94.2% yield).1H NMR (400 MHz, CDCl3): δ 7.75 (d, J = 8.5 Hz, 1H), 6.92 (d, J = 2.2 Hz, 1H), 6.57 (dd, J = 8.5,2.2 Hz, 1H), 4.04 (brs, 2H) and 3.86 (s, 3H) ppm; melting point: 96-98 °C. | [References]
[1] Organic Letters, 2013, vol. 15, # 13, p. 3234 - 3237
[2] Chinese Chemical Letters, 2011, vol. 22, # 12, p. 1411 - 1414
[3] European Journal of Medicinal Chemistry, 2014, vol. 81, p. 59 - 75
[4] Acad. romine Stud. Cerc. Chim., 1956, vol. 4, p. 175,178
[5] Patent: WO2012/93101, 2012, A1. Location in patent: Page/Page column 236-237 |
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