4-Chloroanisole → Ethyl 4'-methoxy[1,1'-biphenyl]-4-carboxylate

HRID 607843Notes

Reaction equation

HRID 607843 reaction equation
CCOC(=O)c1ccc(B(O)O)cc1.COc1ccc(Cl)cc1>C1=C\CC/C=C\CC/1.C1=C\CC/C=C\CC/1.C1COCCO1.Cc1cc(C)c(-c2cc(-c3c(C)cc(C)cc3C)cc(P(c3cc(-c4c(C)cc(C)cc4C)cc(-c4c(C)cc(C)cc4C)c3)C3CCCC3)c2)c(C)c1.O.O=P([O-])([O-])[O-].[K+].[K+].[K+].[Ni]>CCOC(=O)c1ccc(-c2ccc(OC)cc2)cc1

Participants

8

Reactant 2

HCID 121674-ChloroanisoleHCID 27343504-Ethoxycarbonylphenylboronic acid

Product 1

HCID 2764348Ethyl 4'-methoxy[1,1'-biphenyl]-4-carboxylateYield 34%

Reagents, catalysts & solvents 5

HCID 962WaterReagentHCID 62657Potassium Phosphate, TribasicReagentHCID 6433264Bis(1,5-cyclooctadiene)nickelCatalystHCID 178424451HCID 178424451, compoundCatalystHCID 312751,4-DioxaneSolvent4×

Conditions

Temperature
60 °C

Procedure

pre-ligate Ni(cod)2 and phosphine ligand in dioxane for 15 minutes in a separate plate

Workup

  1. additionDilute with acetonitrile
  2. aliquotNo procedure recorded
  3. customDiluent solution was made in 1 L batches with 950 mL acetonitrile, 25 mL water, 25 mL glacial acetic acid, and 53 mg 4,4’-di-tert-butylbiphenyl as an external standard (0.2 equiv standard per reaction). Aliquot taken from each well (47 ul) is added into 753 ul of diluent solution

Sources & evidence

ORD record
ord-06d28a54dec04bc1bd480428c6d3fc9f
Source dataset
Ni-catalyzed Suzuki Miyaura cross-coupling
Original link
View source

Reaction notes

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