反応 #46247

ord-6308b021400e4046b19ed29fea48dfda

反応方程式

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
収率 104.6%

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出The resulting mixture was extracted with EtOAc
  2. 2
    乾燥The organic layer was dried over Na2SO4
  3. 3
    その他evaporated under reduced pressure

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07741321B2uspto-grants-2010_06