Benzonitrile, p-imidazol-1-yl- → HCID 178510012, compound

HRID 1083783Notes

Reaction equation

HRID 1083783 reaction equation
FC(F)(F)c1cncc(Br)c1.N#Cc1ccc(-n2ccnc2)cc1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].CCCCC1(P(C2CCCCC2)C2CCCCC2)c2ccccc2-c2ccccc21.[K+]>N#Cc1ccc(-n2cncc2-c2cncc(C(F)(F)F)c2)cc1

Participants

8

Reactant 2

HCID 135744Benzonitrile, p-imidazol-1-yl-HCID 111279913-Bromo-5-(trifluoromethyl)pyridine

Product 1

HCID 178510012HCID 178510012, compoundYield 3.91%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 71310598(9-Butylfluoren-9-yl)-dicyclohexylphosphaneCatalystHCID 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-862bdcfa07264a0d8a4bc600568d9120
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

Loading…