Basic information Safety Supplier Related

2-AMINO-4-CHLOROPHENYL BORONIC ACID PINACOL ESTER

Basic information Safety Supplier Related

2-AMINO-4-CHLOROPHENYL BORONIC ACID PINACOL ESTER Basic information

Product Name:
2-AMINO-4-CHLOROPHENYL BORONIC ACID PINACOL ESTER
Synonyms:
  • 2-AMINO-4-CHLOROPHENYL BORONIC ACID PINACOL ESTER
  • 2-Amino-4-chlorophenyl boronic acid
  • 5-chloro-2-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)aniline
  • 25G 100G 500G
  • 5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)
  • Benzenamine, 5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS:
863578-21-6
MF:
C12H17BClNO2
MW:
253.53
Mol File:
863578-21-6.mol
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2-AMINO-4-CHLOROPHENYL BORONIC ACID PINACOL ESTER Chemical Properties

Boiling point:
363.6±32.0 °C(Predicted)
Density 
1.15±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
pka
2.84±0.11(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

HS Code 
2931900090
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2-AMINO-4-CHLOROPHENYL BORONIC ACID PINACOL ESTER Usage And Synthesis

Synthesis

823-57-4

25015-63-8

863578-21-6

Step 1: Preparation of 5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline To a solution of 2-bromo-5-chloroaniline (20.0 g, 96.9 mmol) in 1,4-dioxane (200 ml) was sequentially added triethylamine (54.0 ml, 487 mmol) and [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloride dichloromethane complex (3.96 g, 4.84 mmol) under nitrogen protection. Subsequently, 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (42.3 ml, 290 mmol) was slowly added dropwise. The reaction mixture was stirred at 100 °C for 10.5 hours. After completion of the reaction, the mixture was cooled to room temperature and filtered through diatomaceous earth. The filtrate was quenched by dropwise addition of methanol (25 ml) at 0°C. The solvent was removed by concentration under reduced pressure and the resulting crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate = 20:1) to afford the target product 5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (16.5 g, 65% yield). 1H-NMR (400 MHz, DMSO-d6): δ (ppm) 7.28 (1H, d, J=6.0 Hz), 6.59 (1H, d, J=1.2 Hz), 6.43 (1H, dd, J=6.3,1.5 Hz), 5.70 (2H, s), 1.24 (12H, s).

References

[1] Patent: EP1719773, 2006, A1. Location in patent: Example 1-10

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