2-Acetyl-5-bromothiophene → HCID 178466103, compound

HRID 1082848

Reaction equation

HRID 1082848 reaction equation
CC(=O)c1ccc(Br)s1.CC(C)n1ccnc1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].Cc1cc(C)c(-n2ccnc2P(C2CCCCC2)C2CCCCC2)c(C)c1.[K+]>CC(=O)c1ccc(-c2cncn2C(C)C)s1

Participants

8

Reactant 2

HCID 793352-Acetyl-5-bromothiopheneHCID 101761131H-Imidazole, 1-(1-methylethyl)-

Product 1

HCID 178466103HCID 178466103, compoundYield 1.17%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 534118192-(Dicyclohexylphosphanyl)-1-(2,4,6-trimethylphenyl)-1H-imidazoleCatalystHCID 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-a3de1be5a2b7451bb10d58f45b7aac9d
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Linked notes

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