Sodium Carbonate → 1,1'-Biphenyl, 3,5-dibromo-

HRID 339424ノート

反応式

HRID 339424 の反応式
B([O-])([O-])O[C:3]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[CH:4]=1.I[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(=O)([O-])[O-].[Na+].[Na+]>O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Br:10][C:5]1[CH:4]=[C:3]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:8]=[C:7]([Br:9])[CH:6]=1

参加物

6

実験手順

Suspended in 32 ml of 1,2-dimethoxymethane were 3.0 g (11 mmol) of 3,5-dibromophenyl borate, 2.2 g (11 mmol) of iodobenzene and 0.25 g (0.21 mmol) of tetrakis(triphenylphosphine)palladium, and a solution prepared by dissolving 3.4 g (32 mmol) of sodium carbonate in 16 ml of water was added thereto and refluxed for 9 hours under argon atmosphere by heating. The reaction solution was separated into two layers, and then the organic layer separated was washed in order with 5% sodium carbonate, 5% hydrochloric acid, water and saturated brine and dried on anhydrous sodium sulfate. After the organic solvent was distilled off under reduced pressure, the residue was refined by silica gel chromatography (only hexane) to obtain 2.5 g (yield: 75%) of 3,5-dibromobiphenyl (5).

後処理

  1. customa solution prepared
  2. additionwas added
  3. temperaturerefluxed for 9 hours under argon atmosphere
  4. temperatureby heating
  5. customThe reaction solution was separated into two layers
  6. customthe organic layer separated
  7. washwas washed in order with 5% sodium carbonate, 5% hydrochloric acid, water and saturated brine
  8. dry with materialdried on anhydrous sodium sulfate
  9. distillationAfter the organic solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-d027abda632343ce85d845f123177256
出典データセット
uspto-grants-2014_11
特許番号
US08895154B2

反応ノート

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