METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE
METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE Basic information
- Product Name:
- METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE
- Synonyms:
-
- METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE
- SALOR-INT L446718-1EA
- 5-bromo-2-hydroxy-4-methoxyBenzoic acid methyl ester
- Benzoic acid, 5-bromo-2-hydroxy-4-methoxy-, methyl ester
- CAS:
- 39503-52-1
- MF:
- C9H9BrO4
- MW:
- 261.07
- Mol File:
- 39503-52-1.mol
METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE Chemical Properties
- Melting point:
- 143 °C
- Boiling point:
- 328.9±37.0 °C(Predicted)
- Density
- 1.573±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 8.83±0.23(Predicted)
- Appearance
- White to off-white Solid
METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE Usage And Synthesis
Synthesis
98437-41-3
18107-18-1
39503-52-1
A) General procedure for synthesizing methyl 5-bromo-2-hydroxy-4-methoxybenzoate: to a solution of 5-bromo-2-hydroxy-4-methoxybenzoic acid (2.00 g) in methanol (10.0 mL) was slowly added a solution of 0.6 M (diazomethyl)trimethylsilane in hexanes (14.8 mL) under cooling conditions in an ice bath. The reaction mixture was stirred at room temperature for 3 hours. Upon completion of the reaction, acetic acid (0.12 mL) was added to quench the reaction, followed by evaporation of the solvent under reduced pressure. The resulting crude product was purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to afford the target compound methyl 5-bromo-2-hydroxy-4-methoxybenzoate (2.08 g). The product was characterized by 1H NMR (300 MHz, CDCl3) with chemical shifts of δ3.91 (3H, s), 3.93 (3H, s), 6.49 (1H, s), 7.99 (1H, s), 10.93 (1H, s).
References
[1] Patent: WO2015/163485, 2015, A1. Location in patent: Paragraph 0342
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