Abstract
Microwave assisted synthesis of eight electron rich aryl boronates
(2a -c, 4,
6a -d ) via palladium catalyzed
reactions of the corresponding aryl bromides with bis(pinacolato)diboron
are described. Compared to conventional heating conditions, dramatic rate
enhancements were found for reactions carried out under microwave
irradiation, reducing reaction times from hours or days to only
minutes.
Key words
palladium - bis(pinacolato)diboron - arylboronates - microwave irradiation - indoles
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Representative Experimental Procedure.
Synthesis of tris{4-(4,4,5,5-tetra-methyl-[1,3,2]dioxaborolan-2-yl)-phenyl}amine 4: Tris(4-bromophenyl)amine 3 (48
mg, 0.1 mmol), bis(pinacolato)diboron (76 mg, 0.3 mmol), KOAc (88
mg, 0.9 mmol) and Pd(dppf)Cl2 (8 mg, 3 mol%)
were suspended in dry DME (2 mL) in a 10 mL glass tube which was
tightly sealed with an aluminum/Teflon crimp. The sample
was irradiated at 250 W, 150 °C for 17 min in a CEM-Discover
mono-mode microwave apparatus. After completion of the reaction,
the vessel was cooled down to 60 °C and the crude mixture
was filtered through a thin plug of celite. The celite plug was
washed with ether (3 × 5 mL), the organic fractions were
combined and the solvent was removed under reduced pressure. The
resultant crude product was then washed with methanol (× 3)
and recrystallized from a diethyl ether-methanol mixture
to furnish 56 mg (89%) of pure product 4 as
light yellow crystals. m p > 300 °C. 1 H
NMR (300 MHz, CDCl3 ): δ = 1.36 (s,
36 H), 7.10 (d, 6 H), 7.70 (s, 6 H). 13 C
NMR (75 MHz, CDCl3 ): δ = 24.8, 83.6,
123.5, 135.90, 149.8. LR-MS (EI) [M+ ]:
624 (39), 623 (100), 622 (69), 497 (15), 496 (7). HR-MS (EI): C36 H48 B3 NO6 Calcd
623.3760, found. 623.3755.