Sodium Carbonate → [2,2'-Bithiophene]-5-carboxaldehyde

HRID 363521

反応式

HRID 363521 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1B(O)O.C([O-])([O-])=O.[Na+].[Na+].O1CCOCC1.C([C:24]1[S:28][C:27]([CH:29]=[O:30])=[CH:26][CH:25]=1)(O)=O>O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:24]1[S:28][C:27]([CH:29]=[O:30])=[CH:26][CH:25]=1

参加物

7

実験手順

To a solution of thien-2-ylboronic acid (0.939 g, 7.34 mmol) and Na2CO3 (2.40 g, 22.6 mmol) in water (75 mL) is added p-dioxane (75 mL). This mixture is treated sequentially with 5-carboxy-2-thiophenecarboxaldehyde (1.43 g, 7.48 mmol) and palladium (II) acetate (151 mg, 0.673 mmol) and allowed to stir at ambient temperature for 16 hours. The solvent is evaporated in vacuo. To the residue is added EtOAc (400 mL) and water (300 mL). The aqueous layer is acidified to pH 1 with 1.0N aq. HCl. The aqueous layer is extracted with EtOAc (2×200 mL). The organic extracts are combined, washing with brine (200 mL), 5% aq. Na2S2O3 (200 mL), sat. aq. NaCl (200 mL), drying (Na2SO4), and the solvent evaporation in vacuo affords the title compound.

後処理

  1. customThe solvent is evaporated in vacuo
  2. additionTo the residue is added EtOAc (400 mL) and water (300 mL)
  3. extractionThe aqueous layer is extracted with EtOAc (2×200 mL)
  4. washwashing with brine (200 mL), 5% aq. Na2S2O3 (200 mL), sat. aq. NaCl (200 mL)
  5. dry with materialdrying (Na2SO4)
  6. customthe solvent evaporation in vacuo

出典と根拠

ORDレコード
ord-e97527c8980b4262893c7b5db2e97ea9
出典データセット
uspto-grants-1999_02
特許番号
US05874452

関連ノート

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