Ethyl Acetate → 2'-Chloro[1,1'-biphenyl]-4-carbaldehyde

HRID 1394158

反応式

HRID 1394158 の反応式
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[Cl:8].[CH:9]([C:11]1[CH:16]=[CH:15][C:14](B(O)O)=[CH:13][CH:12]=1)=[O:10].C(=O)([O-])[O-].[Na+].[Na+].C(OCC)(=O)C>C1(C)C=CC=CC=1.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>[CH:9]([C:11]1[CH:16]=[CH:15][C:14]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[Cl:8])=[CH:13][CH:12]=1)=[O:10]

参加物

7

実験手順

To a solution of 2-bromochlorobenzene (0.24 mL, 2 mmol) and 4-formylbenzeneboronic acid (0.35 g, 2.2 mmol) in toluene (20 mL) were added 2M aq. sodium carbonate (2.6 mL) followed by (Ph3P)4Pd (0.34 g, 0.3 mmol). The resulting reaction mixture was refluxed for 3 h, cooled and diluted ethyl acetate. The organic phase was washed with water, saturated aq. sodium bicarbonate, brine and dried over sodium sulfate. The filtrate was concentrated in vacuo and the residue obtained was purified by chromatography (hexane:ethyl acetate; 4:1) to yield the title product.

後処理

  1. customThe resulting reaction mixture
  2. temperaturewas refluxed for 3 h
  3. temperaturecooled
  4. washThe organic phase was washed with water, saturated aq. sodium bicarbonate, brine
  5. dry with materialdried over sodium sulfate
  6. concentrationThe filtrate was concentrated in vacuo
  7. customthe residue obtained
  8. customwas purified by chromatography (hexane:ethyl acetate; 4:1)

出典と根拠

ORDレコード
ord-c73cff83589e435d93d15875f07dee8c
出典データセット
uspto-grants-2008_03
特許番号
US07348348B2

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