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Methyl 4-bromo-2-fluorobenzoate

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Company Name: SHANGHAI YINGRUI CHEMICAL TECHNOLOGY CO.,LTD.  Gold
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Methyl 4-bromo-2-fluorobenzoate manufacturers

Methyl 4-bromo-2-fluorobenzoate Basic information
Product Name:Methyl 4-bromo-2-fluorobenzoate
Synonyms:Methyl 4-bromo-2-fluorobenzoate;Fluoro-4-bromobenzoate;Enzalutamide Impurity 15;Enzalutamide EP Impurity C;Benzoic acid, 4-bromo-2-fluoro-, methyl ester;Methyl 4-bromo-2-fluorobenzoate(For export only);Methy 4-bromo-2-fluorobenzoate;Enzalutamide ImpuritiesC
CAS:179232-29-2
MF:C8H6BrFO2
MW:233.03
EINECS:
Product Categories:Aromatic Esters;blocks;Bromides;Carboxes;FluoroCompounds
Mol File:179232-29-2.mol
Methyl 4-bromo-2-fluorobenzoate Structure
Methyl 4-bromo-2-fluorobenzoate Chemical Properties
Melting point 58-60℃
Boiling point 272.7±25.0℃ (760 Torr)
density 1.577±0.06 g/cm3 (20 ºC 760 Torr)
Fp 118.7±23.2℃
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
color White to Off-White
InChIInChI=1S/C8H6BrFO2/c1-12-8(11)6-3-2-5(9)4-7(6)10/h2-4H,1H3
InChIKeyDLILIUSWDLJMCE-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(Br)C=C1F
Safety Information
HS Code 2916399090
MSDS Information
Methyl 4-bromo-2-fluorobenzoate Usage And Synthesis
Chemical Propertiesoff-white powder
Uses4-Bromo-2-fluorobenzoic Acid Methyl Ester is the methyl ester derivative of 4-Bromo-2-fluorobenzoic Acid (B684620) and is used as a reagent in the synthesis of aminopyridyl-based inhibitors targeting Trypanosoma cruzi CYP51 as anti-Chagas agents.
Synthesis
Methanol

67-56-1

4-Bromo-2-fluorobenzoic acid

112704-79-7

Methyl 4-bromo-2-fluorobenzoate

179232-29-2

Step 1: To a stirred solution of 4-bromo-2-fluorobenzoic acid (15.0 g, 68.49 mmol, 1 eq.) in methanol (150 mL) was slowly added thionyl chloride (23.09 mL, 136.9 mmol, 2 eq.) at 0 °C. The reaction mixture was kept at 0 °C for 15 minutes before being brought to room temperature and stirring was continued for 12 hours. After completion of the reaction, methanol was removed by evaporation under reduced pressure and the residue was diluted with ethyl acetate (250 mL). The organic layer was washed sequentially with saturated aqueous sodium bicarbonate solution, brine (150 mL) and deionized water (150 mL). The ethyl acetate layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give methyl 4-bromo-2-fluorobenzoate (15 g, 93% yield) as an off-white solid (LC-MS purity 99%; TLC conditions: ethyl acetate/petroleum ether (3:7), Rf value 0.8).

References[1] Patent: WO2004/46096, 2004, A2. Location in patent: Page 38
[2] Organic Process Research and Development, 2011, vol. 15, # 3, p. 565 - 569
[3] Journal of Medicinal Chemistry, 2013, vol. 56, # 19, p. 7651 - 7668
[4] Patent: WO2015/48306, 2015, A1. Location in patent: Page/Page column 88; 112
[5] Patent: WO2013/68461, 2013, A1. Location in patent: Page/Page column 105; 106; 109
Tag:Methyl 4-bromo-2-fluorobenzoate(179232-29-2) Related Product Information
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