1-Bromo-2-fluorobenzene → HCID 178432950, compound

HRID 1083335Notes

Reaction equation

HRID 1083335 reaction equation
Cc1cn(Cc2ccccc2)c(C)n1.Fc1ccccc1Br>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].COc1ccc(OC)c(P(c2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)c1-c1c(C(C)C)cc(C(C)C)cc1C(C)C.[K+]>Cc1nc(C)n(Cc2ccccc2)c1-c1ccccc1F

Participants

8

Reactant 2

HCID 612591-Bromo-2-fluorobenzeneHCID 147449731-Benzyl-2,4-dimethyl-1H-imidazole

Product 1

HCID 178432950HCID 178432950, compoundYield 2.48%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 44597232Bis(3,5-bis(trifluoromethyl)phenyl)(3,6-dimethoxy-2',4',6'-tri(propan-2-yl)(1,1'-biphenyl)-2-yl)phosphaneCatalystHCID 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-9b5d6f5f876a4ac7bbf0311d9670a310
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

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