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POTASSIUM 3,5-BIS(TRIFLUOROMETHYL)PHENYLTRIFLUOROBORATE

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POTASSIUM 3,5-BIS(TRIFLUOROMETHYL)PHENYLTRIFLUOROBORATE Basic information

Product Name:
POTASSIUM 3,5-BIS(TRIFLUOROMETHYL)PHENYLTRIFLUOROBORATE
Synonyms:
  • potassium [3,5-bis(trifluoromethyl)phenyl]-trifluoroboranuide
  • POTASSIUM 3,5-BIS(TRIFLUOROMETHYL)PHENYLTRIFLUOROBORATE
  • Potassium [3,5-bis(trifluoromethyl)phenyl]trifluoroborate 96%
  • Potassium[3,5-bis(trifluoromethyl)phenyl]trifluoroborate96%
  • Potassium [3,5-bis(trifluoromethyl)pheny]trifluoroborate
  • POTASSIUM 3,5-BIS(TRIFLUOROMETHYL)PHENY&
  • Potassium (3,5-bis(trifluoromethyl)
  • Borate(1-), [3,5-bis(trifluoromethyl)phenyl]trifluoro-, potassium (1:1), (T-4)-
CAS:
166328-09-2
MF:
C8H3BF9K
MW:
320
Product Categories:
  • Aryl
  • Boronic Acids and Derivatives
  • blocks
  • Trifluoroborates
  • Trifluoroborate Salts
  • Molander Ates
  • Organoborons
  • Aryl Trifluoroborate Salts
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Organometallic Reagents
  • Trifluoroborate Salts
Mol File:
166328-09-2.mol
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POTASSIUM 3,5-BIS(TRIFLUOROMETHYL)PHENYLTRIFLUOROBORATE Chemical Properties

Melting point:
>300℃
storage temp. 
Inert atmosphere,Room Temperature
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
2931900090

MSDS

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POTASSIUM 3,5-BIS(TRIFLUOROMETHYL)PHENYLTRIFLUOROBORATE Usage And Synthesis

Synthesis

A solution of 3,5-bis(triflfluoromethyl)phenylboronic acid (10 g, 38.8 mmol) in methanol (15 mL) was added to an aqueous solution of KHF2 (4.5 M, 26 mL, 117 mmol) at room temperature. A heavy precipitate was deposited. The resulting suspension was stirred 148 MODERN ORGANIC SYNTHESIS IN THE LABORATORYfor 1 h at room temperature, and the precipitated product was collected and washed with methanol. Recrystallization from a minimum amount of acetone produced 11 g (89%) of potassium 3,5-bis(triflfluoromethyl)phenyltriflfluoroborate. Reference: Molander, G. A.; Biolatto, B. J. Org. Chem. 2003, 68, 4302−4314.

Uses

Thos chemical has been used for inserting a 3,5-bis(trifluoromethyl)phenyl group into the position of a halogen or triflate group of various arenes and various heterocycles in Pd-catalyzed Suzuli-Miyaura cross-coupling reactions.

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