Benzofuran, 5-bromo- → HCID 178440018, compound

HRID 1082797

Reaction equation

HRID 1082797 reaction equation
Brc1ccc2occc2c1.CC(C)c1nccn1C>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].CN(C)c1ccc(P(C2CCCCC2)C2CCCCC2)cc1.[K+]>CC(C)c1ncc(-c2ccc3occc3c2)n1C

Participants

8

Reactant 2

HCID 90015Benzofuran, 5-bromo-HCID 130729731-Methyl-2-(propan-2-yl)-1H-imidazole

Product 1

HCID 178440018HCID 178440018, compoundYield 65.05%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 142458Benzenamine, 4-(dicyclohexylphosphino)-N,N-dimethyl-CatalystHCID 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-e47419a183bc40408749ae2c4e8f9edc
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Linked notes

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