Water → 3-(1H-indol-5-yl)benzaldehyde
Reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.[CH:11]([C:13]1[CH:14]=[C:15](B(O)O)[CH:16]=[CH:17][CH:18]=1)=[O:12].C(=O)([O-])[O-].[Cs+].[Cs+].O.C(Cl)Cl>O1CCOCC1>[NH:7]1[C:8]2[C:4](=[CH:3][C:2]([C:17]3[CH:18]=[C:13]([CH:14]=[CH:15][CH:16]=3)[CH:11]=[O:12])=[CH:10][CH:9]=2)[CH:5]=[CH:6]1Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
A mixture of 5-bromo-indole (8.7 g, 44.4 mmol), 3-formylbenzeneboronic acid (10 g, 66.7 mmol), cesium carbonate in water (2M, 88.8 mL, 178 mmol) in 450 mL of dioxane was degassed (evacuate in vacuo and pressurize with nitrogen, 3 times) PdCl2(dppf).DCM (1.1 g, 1.3 mmol) was added and the mixture degassed one more time as described above. The resulting mixture was heated at 100° C. for 3 h, then it was allowed to cool to room temperature and partitioned between diethyl ether and water. The aqueous phase was extracted with diethyl ether and the combined organic phases were washed with water, brine, dried over MgSO4, filtered and evaporated to give the crude product. Chromatography on silica gel (elution with ethyl acetate/heptane) afforded 5.6 g of the desired product.
Workup
- customwas degassed (evacuate in vacuo and pressurize with nitrogen, 3 times) PdCl2(dppf)
- customthe mixture degassed one more time
- temperatureto cool to room temperature
- custompartitioned between diethyl ether and water
- extractionThe aqueous phase was extracted with diethyl ether
- washthe combined organic phases were washed with water, brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated
- customto give the crude product
Sources & evidence
- ORD record
- ord-74975e79ff8344c088816e1c27e1b5e0
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07618650B2
Reaction notes
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