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2-Bromo-3-fluorobenzoic acid

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CAS:132715-69-6
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Products Intro: Product Name:2-Bromo-3-fluorobenzoic acid
CAS: 132715-69-6
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2-Bromo-3-fluorobenzoic acid manufacturers

2-Bromo-3-fluorobenzoic acid Basic information
Product Name:2-Bromo-3-fluorobenzoic acid
Synonyms:2-BROMO-3-FLUOROBENZOIC ACID;2-Bromo-3-fluorobenzoic acid 98%;3-Fluoro-2-Bromo Benzoic Acid 2-Bromo-3-Fluorobenzoic Acid;3-Fluoro-2-Bromo Benzoic Acid;2-Bromo-3-fluorobenzoic;BUTTPARK 22\01-97;Benzoic acid, 2-broMo-3-fluoro-;EOS-61551
CAS:132715-69-6
MF:C7H4BrFO2
MW:219.01
EINECS:630-221-3
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Acids and Derivatives;Halides;Fluorine series;Benzoic acid;Benzoic acid series
Mol File:132715-69-6.mol
2-Bromo-3-fluorobenzoic acid Structure
2-Bromo-3-fluorobenzoic acid Chemical Properties
Melting point 158-160°C
Boiling point 292.7±25.0 °C(Predicted)
density 1.789±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka2.51±0.10(Predicted)
color White to Light yellow to Light orange
InChIInChI=1S/C7H4BrFO2/c8-6-4(7(10)11)2-1-3-5(6)9/h1-3H,(H,10,11)
InChIKeyKQRCBMPPEPNNDS-UHFFFAOYSA-N
SMILESC(O)(=O)C1=CC=CC(F)=C1Br
CAS DataBase Reference132715-69-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-36-22
Safety Statements 26-36/37/39-37
HazardClass IRRITANT
HS Code 29163990
MSDS Information
2-Bromo-3-fluorobenzoic acid Usage And Synthesis
Chemical PropertiesOff-white powder
Synthesis Reference(s)Tetrahedron Letters, 36, p. 881, 1995 DOI: 10.1016/0040-4039(94)02385-O
Synthesis
2-Amino-3-fluorobenzoic acid

825-22-9

2-Bromo-3-fluorobenzoic acid

132715-69-6

The general procedure for the synthesis of 2-bromo-3-fluorobenzoic acid from 2-amino-3-fluorobenzoic acid is as follows: in a 1L three-necked round-bottomed flask equipped with a dropping funnel and a thermometer, 20g (0.13 mol) of 2-amino-3-fluorobenzoic acid and 160mL of acetonitrile were added. After the mixture was cooled to 0 °C, 160 mL of 47% hydrobromic acid solution was added slowly and dropwise over 10 min. Subsequently, a solution prepared from 10 g (0.145 mol) of sodium nitrite (NaNO2) dissolved in 20 mL of water was added dropwise to the reaction system over 1 hour. After the dropwise addition, the reaction mixture was continued to be stirred at 0°C for 5 min. Next, 21.8 g (0.15 mol) of copper bromide (CuBr) was added in batches over 30 minutes. The reaction mixture was transferred to a 70°C oil bath and stirred continuously for 1 hour. Upon completion of the reaction, the mixture was cooled to 0 °C, diluted with 700 mL of water and the precipitate was collected by filtration. The precipitate was washed with cold water and dried under vacuum to give the orange solid product 2-bromo-3-fluorobenzoic acid in a yield of 22 g and 78%.

References[1] Patent: US2008/293708, 2008, A1. Location in patent: Page/Page column 37
[2] Journal of Heterocyclic Chemistry, 1990, vol. 27, # 7, p. 2151 - 2163
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