Bromine → 4-Bromo-2-(trifluoromethoxy)phenol

HRID 271649

反応式

HRID 271649 の反応式
[Br:1]Br.[F:3][C:4]([F:14])([F:13])[O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[OH:12].[O-]S([O-])=O.[Na+].[Na+]>C(Cl)Cl>[Br:1][C:10]1[CH:9]=[CH:8][C:7]([OH:12])=[C:6]([O:5][C:4]([F:13])([F:14])[F:3])[CH:11]=1

参加物

5

反応物 3

HCID 24408BromineHCID 24437Sodium SulfiteHCID 27772992-(Trifluoromethoxy)phenol

生成物 1

HCID 117801514-Bromo-2-(trifluoromethoxy)phenol

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒3 回

実験手順

1.55 mL (30.3 mmol) bromine in 50 mL DCM is added dropwise to a solution of 5.0 g (28.1 mmol) 2-trifluoromethoxy-phenol in 70 mL DCM at −78° C. The reaction solution is heated to RT and stirred for a further 48 h. Then 70 mL Na2SO3 solution are added and the mixture is stirred until the orange colour has disappeared. The solution is diluted with DCM, the organic phase is washed with NaCl solution, dried over MgSO4 and the solvent is eliminated i.vac. The purification is carried out by column chromatography on silica gel (gradient: PE to PE:EtOAc 4:1).

後処理

  1. stirringthe mixture is stirred until the orange colour
  2. washthe organic phase is washed with NaCl solution
  3. dry with materialdried over MgSO4
  4. customThe purification

出典と根拠

ORDレコード
ord-bcf3a28d542a4787bc28760aa1133a9a
出典データセット
uspto-grants-2008_11
特許番号
US07452911B2

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