1-Bromo-2-fluorobenzene → HCID 178526665, compound

HRID 1083561Notes

Reaction equation

HRID 1083561 reaction equation
Fc1ccccc1Br.O=[N+]([O-])c1ccc(-n2ccnc2-c2ccccc2)cc1>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+]>O=[N+]([O-])c1ccc(-n2c(-c3ccccc3F)cnc2-c2ccccc2)cc1

Participants

8

Reactant 2

HCID 612591-Bromo-2-fluorobenzeneHCID 11173122HCID 11173122, compound

Product 1

HCID 178526665HCID 178526665, compoundYield 60.49%

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-4a01a42fb4ee489b824bc10cb775b8dd
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

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