Hydrochloric Acid → 3,5-Dichlorophenylboronic acid

HRID 1740284

反応式

HRID 1740284 の反応式
Br[C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[CH:3]=1.C([O:13][B:14](OC(C)C)[O:15]C(C)C)(C)C.C([Li])CCC.Cl>O1CCCC1.CCCCCC>[Cl:9][C:4]1[CH:3]=[C:2]([B:14]([OH:15])[OH:13])[CH:7]=[C:6]([Cl:8])[CH:5]=1

参加物

7

反応条件

温度
-78 °C

実験手順

To a cold (-78° C.) solution of 1-bromo-3,5-dichlorobenzene (14 g) and triisopropoxyborane (20.8 ml) in tetrahydrofuran (140 ml) was added dropwise n-butyllithium in hexane (1.66 M, 52.3 ml). The mixture was stirred at -78° C. for one hour and warmed to room temperature over two hours. The reaction mixture was poured onto 2M hydrochloric acid solution (120 ml) and stirred for 10 minutes. The product was extracted with ether (200 ml) 3 times, and the organic layers were combined, washed with brine, dried over magnesium sulfate and evaporated in vacuo. To the residue was added petroleum ether and the crystalline was collected, washed with petroleum ether and dried to give 3,5-dichlorophenyl-dihydroxyborane.

後処理

  1. temperaturewarmed to room temperature over two hours
  2. stirringstirred for 10 minutes
  3. extractionThe product was extracted with ether (200 ml) 3 times
  4. washwashed with brine
  5. dry with materialdried over magnesium sulfate
  6. customevaporated in vacuo
  7. additionTo the residue was added petroleum ether
  8. customthe crystalline was collected
  9. washwashed with petroleum ether
  10. customdried

出典と根拠

ORDレコード
ord-3b868a2f93d7475d853d55e381fe8c10
出典データセット
uspto-grants-1999_10
特許番号
US05968985

関連ノート

読み込み中…