Bromine → 4-Bromo-2-[(trifluoromethyl)sulfanyl]phenol

HRID 638953ノート

反応式

HRID 638953 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][C:9]([F:12])([F:11])[F:10].[Br:13]Br>C(Cl)Cl.O>[Br:13][C:5]1[CH:6]=[CH:7][C:2]([OH:1])=[C:3]([S:8][C:9]([F:12])([F:10])[F:11])[CH:4]=1

参加物

5

反応条件

温度
-78 °C

実験手順

To a stirred solution of 1-hydroxy-2-trifluoromethylthiobenzene (16 mmol, 1.0 eq.) in CH2Cl2 (40 mL) at −78° C. was added a solution of Br2 (0.83 mL, 16 mmol, 1.0 eq.) in CH2Cl2 (18 mL) slowly. The resulting mixture was stirred at −78° C. for 2 h and then warmed to room temperature overnight. The reaction mixture was diluted with water (300 mL) and extracted with CH2Cl2 (3×150 mL). The combined organic layer was washed with brine (400 mL), dried (Na2SO4) and concentrated in vacuo. The crude product was purified by column chromatography using 0-10% EtOAc in hexanes as an eluent to afford 4-bromo-1-hydroxy-2-trifluoromethylthiobenzene in 93% yield as a crystalline solid.

後処理

  1. temperaturewarmed to room temperature overnight
  2. extractionextracted with CH2Cl2 (3×150 mL)
  3. washThe combined organic layer was washed with brine (400 mL)
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated in vacuo
  6. customThe crude product was purified by column chromatography

出典と根拠

ORDレコード
ord-ffeb37b852f64469997f16b077af38bf
出典データセット
uspto-grants-2010_04
特許番号
US07691843B2

反応ノート

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