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Location:Home > Product > 153766-81-5

153766-81-5 Potassium Phenyltrifluoroborate



 MDL Number: MFCD01318172
 MW: 184.01
 Purity: 97+%
 Product Description:
 Relevant Medicine Name: -
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Accela SY001020 1g 10.00 - - 5 0 3-4days
Accela SY001020 5g 25.00 - - 2 0 3-4days
Accela SY001020 10g 45.00 - - >5 0 3-4days
Accela SY001020 25g 90.00 - - 3 1 0-1day
Accela SY001020 100g 290.00 - - 0 0 inquire

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Treatment with TMS chloride in acetonitrile generates the Lewis acid phenylboron difluoride in situ, avoiding the need to handle boron trihalides: J. Org. Chem., 60, 3020 (1995).
Aryltrifluoroborate salts are more nucleophilic than the corresponding arylboronic acids and undergo ligand-free Pd-catalyzed cross-coupling reactions with arenediazonium tetrafluoroborates to give good yields of biaryls: Tetrahedron Lett., 38, 4393 (1997); Eur. J. Org. Chem., 1875 (1999). Cross-coupling with aryl or heteroaryl halides and triflates, under ligand-free conditions, has subsequently been reported: Org. Lett., 4, 1867 (2002).
Coupling with diaryliodonium salts has also been reported: Synth. Commun., 29, 2457 (1999). The method has been extended to the synthesis of benzophenones by carbonylative cross-coupling in the presence of CO: J. Chem. Res. (Synop.), 400 (1999).
In the presence of Dicarbonyl-(2,4-pentanedionato)-rhodium(I)-, K aryl- and alkenyltrifluoroborates add to aldehydes and enones to give secondary alcohols and saturated ketones, respectively: Org. Lett., 1, 1683 (1999).
Asymmetric Rh-catalyzed additions to enones in the presence of a chiral BINAP catalyst give the corresponding saturated ketones in high yield and ee: Eur. J. Org. Chem., 3552 (2002).
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