Benzofuran, 5-bromo- → HCID 178481276, compound

HRID 1084102Notes

Reaction equation

HRID 1084102 reaction equation
Brc1ccc2occc2c1.Cn1cnc(C#N)c1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].CCP(CC)c1ccccc1-n1c2ccccc2c2ccccc21.[K+]>Cn1cnc(C#N)c1-c1ccc2occc2c1

Participants

8

Reactant 2

HCID 90015Benzofuran, 5-bromo-HCID 27951151-Methyl-1H-imidazole-4-carbonitrile

Product 1

HCID 178481276HCID 178481276, compoundYield 54.08%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 1188786229-[2-(Diethylphosphino)phenyl]-9H-carbazoleCatalystHCID 178455864HCID 178455864, compoundCatalystHCID 31374DimethylacetamideSolvent3×HCID 741954,4'-Bis(1,1-dimethylethyl)-1,1'-biphenylInternal standard

Conditions

Temperature
120 °C

Workup

  1. temperatureCool to room temperature
  2. additionNo procedure recorded
  3. aliquotNo procedure recorded
  4. filtrationFilter into HPLC analysis plate · Keep liquid/mobile
  5. washwash filter with 400 microliter of acetonitrile/water (4:1)

Sources & evidence

ORD record
ord-7ad9a00e347b4d1496b7d4bdc955b436
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

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