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4-(2,2,2-TRIFLUOROETHOXY)PHENYLBORONIC ACID

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4-(2,2,2-TRIFLUOROETHOXY)PHENYLBORONIC ACID Basic information

Product Name:
4-(2,2,2-TRIFLUOROETHOXY)PHENYLBORONIC ACID
Synonyms:
  • 4-(2,2,2-TRIFLUOROETHOXY)PHENYLBORONIC ACID
  • 4-(2,2,2-Trifluoroethoxy)benzeneboronic acid
  • 4-(2,2,2-Trifluoroethoxy)benzeneboronic acid 98%
  • 4-(2,2,2-Trifluoroethoxy)benzeneboronicacid98%
  • (4-(2,2,2-Trifluoroethoxy)
  • Boronic acid, B-[4-(2,2,2-trifluoroethoxy)phenyl]-
  • 4-(2,2,2-trifluoroethoxy)phenyboronic acid
  • 4-(2,2,2-Trifluoroethoxy)benzeneboronic acid, [4-(2,2,2-Trifluoroethoxy)phenyl]boronic acid
CAS:
886536-37-4
MF:
C8H8BF3O3
MW:
219.95
Product Categories:
  • Boronate Ester
  • Boronic Acid
  • blocks
  • BoronicAcids
  • FluoroCompounds
  • Potassium Trifluoroborate
Mol File:
886536-37-4.mol
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4-(2,2,2-TRIFLUOROETHOXY)PHENYLBORONIC ACID Chemical Properties

Melting point:
191-194℃
Boiling point:
297.1±50.0 °C(Predicted)
Density 
1.35±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
8.58±0.16(Predicted)
color 
White
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2931900090
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4-(2,2,2-TRIFLUOROETHOXY)PHENYLBORONIC ACID Usage And Synthesis

Uses

4-(2,2,2-Trifluoroethoxy)phenylboronic acid can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Synthesis

2- (2,2,2-trifluoroethoxy) bromobenzene 2558, isopropyl borate 2448 and methylTetrahydrofuran 1.5L was added to the reaction flask, and the reaction system was cooled to -15 ° C. 500 mL of isopropylmagnesium chloride in tetrahydrofuran (2.0 M) was added dropwise to the above reaction system and the internal temperature was controlled to not more than -10 ° C, and the reaction was kept at a low temperature for 1 hour. After completion of the reaction, 500 mL of 6M aqueous hydrochloric acid solution was added to terminate the reaction and the ρH- = 2 ~ 3 was added, and the mixture was thoroughly stirred and the aqueous phase was extracted with methyltetrahydrofuran (1.5 LX 1). The combined organic layers were washed with saturated brine (1.5 LX 2), and the combined organic layers were dried over anhydrous sodium sulfate and concentrated to give the crude product of 2- (2,2,2-trifluoroethoxy) phenylboronic acid. The crude product was recrystallized from 770 mL of isopropanol and water (10: 1 by volume) to give 187 g of 2- (2,2,2-trifluoroethoxy) phenylboronic acid in a molar yield of 85%.

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