4'-Methoxyacetophenone → 1-(4-Methoxyphenyl)ethanol

HRID 1484229Notes

Reaction equation

HRID 1484229 reaction equation
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[CH:6][CH:5]=1)=[O:3].C[Si](C)(C)O[SiH](C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1C=CC=CC=1.C1COCC1>[CH3:11][O:10][C:7]1[CH:8]=[CH:9][C:4]([CH:2]([OH:3])[CH3:1])=[CH:5][CH:6]=1

Participants

6

Procedure

A 30-mL eggplant flask equipped with a magnetic stirrer was heat dried while pumping to a vacuum of 5 Pa before its interior was purged with nitrogen atmosphere. To the flask, 4-methoxyacetophenone (151 mg, 1.0 mmol) and 1,1,1,3,3-pentamethyldisiloxane (372 mg, 2.5 mmol) were added through a syringe, and dissolved in benzene (0.5 mL). To the solution, iron complex A (5.0 mg, 0.01 mmol) was added as catalyst. The solution was stirred at room temperature for 6 hours. At 0° C., tetrabutylammonium fluoride in THF (1 M, 1 mL) was then added to the solution, which was stirred at 0° C. for 1 hour. The solvents were distilled off in vacuum. The crude product was purified by silica gel-packed column chromatography using hexane/ethyl acetate (3/1) as developing solvent, obtaining 1-(4-methoxyphenyl)ethanol (140 mg, 0.92 mmol, 92%). The results are shown as Entry 1 in Table 7. The resulting alcohol was identified for geometry by 1H and 13C-NMR spectroscopy.

Workup

  1. customA 30-mL eggplant flask equipped with a magnetic stirrer
  2. temperaturewas heat
  3. customdried
  4. customwas purged with nitrogen atmosphere
  5. additionTo the solution, iron complex A (5.0 mg, 0.01 mmol) was added as catalyst
  6. stirringwas stirred at 0° C. for 1 hour
  7. distillationThe solvents were distilled off in vacuum
  8. customThe crude product was purified by silica gel-

Sources & evidence

ORD record
ord-28a27c517c2d4a628ee1aeec73e23ae0
Source dataset
uspto-grants-2016_08
Patent number
US09421532B2

Reaction notes

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