Phenol → Chroman

HRID 1858032Notes

Reaction equation

HRID 1858032 reaction equation
[C:1]1(O)[CH:6]=[CH:5]C=[CH:3][CH:2]=1.B(F)(F)F.[CH3:12][CH2:13][O:14][CH2:15][CH3:16].O1CCOCC1>C(OCC)C>[O:14]1[C:15]2[C:6](=[CH:1][CH:2]=[CH:3][CH:16]=2)[CH2:5][CH2:12][CH2:13]1

Participants

5

Procedure

To a solution of phenol 4 (0.01 mol) and a catalyst, preferably boron trifluoride diethyl etherate (0.016 mol) in an organic solvent, preferably dry dioxane (10 mL), is added vinyl lactone 2 (0.016 mol) in an organic solvent, preferably dry dioxane (5.0 mL) over 1-60 minutes, preferably 60 minutes at 0-150° C., preferably 110° C., under an inert gas. The reaction mixture is stirred for 0 to 8 hours, preferably 0 hours, at the selected temperature, cooled to room temperature, and diluted with an organic solvent, preferably diethyl ether (200 mL). The reaction mixture is then washed with water (100 mL, 2×50 mL), dried over sodium sulfate (Na2SO4), and solvent is removed under reduced pressure to afford a brown oily residue. The residue is dissolved in alcohol, preferably methanol (30 mL), and the alcohol is then removed under reduced pressure. The brown oily liquid or semisolid is further purified by chromatography, preferably on silica gel, to afford pure racemic chroman derivative 5.

Workup

  1. custompreferably 60 minutes
  2. customat 0-150° C.
  3. custompreferably 110° C.
  4. washThe reaction mixture is then washed with water (100 mL, 2×50 mL)
  5. dry with materialdried over sodium sulfate (Na2SO4), and solvent
  6. customis removed under reduced pressure
  7. customto afford a brown oily residue
  8. custompreferably methanol (30 mL), and the alcohol is then removed under reduced pressure
  9. customThe brown oily liquid or semisolid is further purified by chromatography, preferably on silica gel

Sources & evidence

ORD record
ord-6f990c3d8a884befb0b60cdb88df326f
Source dataset
uspto-grants-2000_11
Patent number
US06150402

Reaction notes

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