4-Chloroanisole → 4-Methoxybiphenyl

HRID 227854

Reaction equation

HRID 227854 reaction equation
[OH-].[OH-].[C:3]1([B+2])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].Cl[C:19]1[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(P(C2CCCCC2)C2C=CC3C(=CC=CC=3)C=2C2C3C(=CC=CC=3)C=CC=2P(C2CCCCC2)C2CCCCC2)CCCCC1.O1CCOCC1>[CH3:26][O:25][C:22]1[CH:23]=[CH:24][C:19]([C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=2)=[CH:20][CH:21]=1

Participants

7

Procedure

An oven dried resealable Schlenk tube was purged with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 0.5 mol %), ligand 2 [Example 1] (5.9 mg, 0.015 mmol, 0.75 mol %), phenylboron dihydroxide (366 mg, 3.0 mmol), and potassium phosphate (850 mg, 4.0 mmol). The tube was purged with argon, and dioxane (6 mL), and 4-chloroanisole (0.24 mL, 2.0 mmol) were added through a rubber septum. The septum was removed, the tube was sealed with a teflon screw cap and the mixture was stirred at room temperature for two minutes, then heated to 100° C. with stirring until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (40 mL) and poured into a separatory funnel. The mixture was washed with 1M NaOH (40 mL), and the layers were separated. The aqueous layer was extracted with ether (40 mL), and the combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was then purified by flash chromatography on silica gel to give 347 mg (94%) of a white solid.

Workup

  1. customAn oven dried resealable Schlenk tube
  2. customwas purged with argon
  3. additionwere added through a rubber septum
  4. customThe septum was removed
  5. customthe tube was sealed with a teflon
  6. customscrew cap
  7. temperatureheated to 100° C.
  8. stirringwith stirring until the starting aryl chloride
  9. customhad been completely consumed
  10. additionThe reaction mixture was then diluted with ether (40 mL)
  11. additionpoured into a separatory funnel
  12. washThe mixture was washed with 1M NaOH (40 mL)
  13. customthe layers were separated
  14. extractionThe aqueous layer was extracted with ether (40 mL)
  15. dry with materialthe combined organic extracts were dried over anhydrous magnesium sulfate
  16. filtrationfiltered
  17. concentrationconcentrated in vacuo
  18. customThe crude material was then purified by flash chromatography on silica gel

Sources & evidence

ORD record
ord-9a94bd1a2b484dd5b18da8004731f986
Source dataset
uspto-grants-2009_07
Patent number
US07560582B2

Linked notes

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