Reacción #46247

ord-6308b021400e4046b19ed29fea48dfda

Ecuación de reacción

Cl
HCl
CNS(=O)(=O)c1ccc(Br)cc1
4-bromo-N-methyl-benzene sulfonamide
CC(C)OB(OC(C)C)OC(C)C
B(OiPr)3
[Li][CH2]CCC
n-BuLi
CNS(=O)(=O)c1ccc(B(O)O)cc1
4-(N-methylsulfamoyl)phenylboronic acid
Rendimiento 104.6%

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ExtracciónThe resulting mixture was extracted with EtOAc
  2. 2
    SecadoThe organic layer was dried over Na2SO4
  3. 3
    Otroevaporated under reduced pressure

Procedimiento

To a solution of 4-bromo-N-methyl-benzene sulfonamide (24.9 g, 0.1 mol) and B(OiPr)3 (28.2 g, 0.15 mol) in THF (200 mL) was added n-BuLi (100 mL, 0.25 mol) at −70° C. The mixture was slowly warmed to 0° C., then 10% HCl solution was added until pH 3˜4. The resulting mixture was extracted with EtOAc. The organic layer was dried over Na2SO4, and evaporated under reduced pressure to give 4-(N-methylsulfamoyl)phenylboronic acid (22.5 g, 96%), which was used in the next step without further purification. 1H NMR (DMSO-d6, 300 MHz) δ 8.29 (s, 2H), 7.92 (d, J=8.1 Hz, 2H), 7.69 (d, J=8.4 Hz, 2H), 2.36 (d, J=5.1 Hz, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07741321B2uspto-grants-2010_06