Benzofuran, 5-bromo- → HCID 178456430, compound

HRID 1083393Notes

Reaction equation

HRID 1083393 reaction equation
Brc1ccc2occc2c1.CC(C)n1ccnc1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].CC12CC3(C)OC(C)(CC(C)(O1)P3c1ccccc1)O2.[K+]>CC(C)n1cncc1-c1ccc2occc2c1

Participants

8

Reactant 2

HCID 90015Benzofuran, 5-bromo-HCID 101761131H-Imidazole, 1-(1-methylethyl)-

Product 1

HCID 178456430HCID 178456430, compoundYield 23.32%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 534277901,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantaneCatalystHCID 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-602fd63dedc34a31a7c5f63366f88593
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

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