1-Methylimidazole → HCID 178481233, compound

HRID 1083498Notes

Reaction equation

HRID 1083498 reaction equation
Brc1ccc2occc2c1.Cn1ccnc1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=C(c1ccccc1)c1ccccc1)P(C1CCCCC1)C1CCCCC1.CC(=O)N(C)C.CC(C)(C)C(=O)[O-].[K+]>Cn1cncc1-c1ccc2occc2c1

Participants

8

Reactant 2

HCID 13901-MethylimidazoleHCID 90015Benzofuran, 5-bromo-

Product 1

HCID 178481233HCID 178481233, compoundYield 62.92%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 12010824Cy-vBRIDPCatalystHCID 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-42f64c332de94d40924a1970f9f4a90b
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

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