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4-Amino-3-fluorophenylboronic acid, pinacol ester

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4-Amino-3-fluorophenylboronic acid, pinacol ester Basic information

Product Name:
4-Amino-3-fluorophenylboronic acid, pinacol ester
Synonyms:
  • 4-Amino-3-fluorophenylboronic acid, pinacol ester
  • 4-AMino-3-fluorobenzeneboronic acid pinacol ester, 96%
  • 2-fluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzenaMine
  • 2-Fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenylamine
  • 2-fluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)aniline
  • 2-fluoro-4-(4
  • Benzenamine, 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anil...
CAS:
819058-34-9
MF:
C12H17BFNO2
MW:
237.08
Mol File:
819058-34-9.mol
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4-Amino-3-fluorophenylboronic acid, pinacol ester Chemical Properties

Melting point:
102-104°C
Boiling point:
334℃
Density 
1.11
Flash point:
156℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Sparingly), DMSO (Sparingly), Methanol (Slightly)
pka
2.84±0.10(Predicted)
form 
Solid
color 
Pale Orange to Light Brown
Sensitive 
Air Sensitive
InChIKey
AIXGNRNTXUKZLC-UHFFFAOYSA-N
CAS DataBase Reference
819058-34-9
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HS Code 
2931900090
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4-Amino-3-fluorophenylboronic acid, pinacol ester Usage And Synthesis

Synthesis

29632-74-4

73183-34-3

819058-34-9

General procedure for the synthesis of 4-amino-3-fluorophenylboronic acid pinacol ester from 2-fluoro-4-iodoaniline and bis(pinacolato) borate: 1. 2-Fluoro-4-iodoaniline (5.0 g, 21.1 mmol) and bis(pinacolato)ethylborane (5.89 g, 23.2 mmol) were dissolved in 130 mL of DMSO under argon protection. 2. Potassium acetate (6.21 g, 63.3 mmol) was added and argon was continuously passed for 10 minutes to exclude oxygen. 3. a 1:1 complex of [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloride (1.21 g, 1.50 mmol) with dichloromethane was added, and the reaction mixture was heated at 85 °C for 4.5 hours. 4. After the reaction was complete, it was cooled to room temperature and diluted with 500 mL of water. 5. The mixture was extracted with ethyl acetate (3 x 200 mL), the organic phases were combined, washed with water, dried over anhydrous sodium sulfate, and then concentrated to dryness under reduced pressure. 6. The crude product was purified by silica gel column chromatography with cyclohexane/ethyl acetate (90/10, v/v) as eluent. 7. 3.73 g of white powder was obtained in 75% yield. 8. The product had a melting point of 11.0%. 8. The melting point of the product was 112 °C. 9. 9. 1H NMR (400 MHz, CDCl3) data: δ (ppm): 1.2 (s, 12H); 3.8 (br s, 2H); 6.55 (t, 1H, J=7Hz); 7.25-7.35 (m, 2H).

References

[1] Patent: US2013/178472, 2013, A1. Location in patent: Paragraph 0239; 0240
[2] Patent: WO2008/32086, 2008, A1. Location in patent: Page/Page column 110
[3] Patent: WO2006/113432, 2006, A2. Location in patent: Page/Page column 66
[4] Patent: WO2008/32086, 2008, A1. Location in patent: Page/Page column 110

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