Gamma-Butyrolactone → 4-Hydroxy-1-phenylbutan-1-one

HRID 2421406Notes

Reaction equation

HRID 2421406 reaction equation
[O:1]1[CH2:5][CH2:4][CH2:3][C:2]1=[O:6].[C:7]1([Li])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C(OCC)C>[OH:1][CH2:5][CH2:4][CH2:3][C:2]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:6]

Participants

4

Conditions

Temperature
-78 °C

Procedure

To a solution of dihydrofuran-2-one (5.71 g, 66 mmol) in diethyl ether (70 mL) at −78° C. was slowly added phenyl lithium (24 mL, 40 mmol, 1.67 M solution in cyclohexane/diethyl ether). After stirring at −78° C. for 2 hours, the reaction mixture was quenched by the addition of 10% NH4Cl (35 mL). The mixture was warmed to room temperature and the layers separated. The aqueous layer was extracted with diethyl ether (2×40 mL). The combined organics were washed with water (2×40 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography (2:3 hexanes/ethyl acetate) to provide the product (6.4 g, 97%) as pale yellow oil.

Workup

  1. customat −78° C.
  2. customthe reaction mixture was quenched by the addition of 10% NH4Cl (35 mL)
  3. temperatureThe mixture was warmed to room temperature
  4. customthe layers separated
  5. extractionThe aqueous layer was extracted with diethyl ether (2×40 mL)
  6. washThe combined organics were washed with water (2×40 mL)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by flash column chromatography (2:3 hexanes/ethyl acetate)

Sources & evidence

ORD record
ord-404e71dbe26947c2ad0b8b7cac0159ef
Source dataset
uspto-grants-2011_06
Patent number
US07956073B2

Reaction notes

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