1-(4-Fluoro-3-methoxyphenyl)ethanone → (αR)-4-Fluoro-3-methoxy-α-methylbenzenemethanol

HRID 1446584Notes

Reaction equation

HRID 1446584 reaction equation
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([F:10])=[C:6]([O:11][CH3:12])[CH:5]=1)=[O:3].B(Cl)([C@@H]1[C@H](C)[C@@H]2C(C)(C)[C@@H](C2)C1)[C@@H]1[C@H](C)[C@@H]2C(C)(C)[C@@H](C2)C1>C1COCC1>[F:10][C:7]1[CH:8]=[CH:9][C:4]([C@H:2]([OH:3])[CH3:1])=[CH:5][C:6]=1[O:11][CH3:12]

Participants

4

Conditions

Temperature
-20 °C

Procedure

A solution of 4-fluoro-3-methoxyacetophenone (1 g) in THF (10 mL) was added dropwise to a solution of (+)-DIPCl™ (2.29 g) in THF (30 mL) in a nitrogen atmosphere at −20° C., and the reaction solution was stirred at −20° C. for 5 hours. The reaction solution was heated to room temperature, and the solvent was evaporated under reduced pressure. The residue was diluted with an ether, diethanolamine (1.25 mL) was added to the diluent, and the reaction solution was stirred at room temperature overnight. The reaction solution was filtered on a celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent:heptane-ethyl acetate system) to obtain 918 mg of the title compound. The physical properties of the compound are as follows.

Workup

  1. temperatureThe reaction solution was heated to room temperature
  2. customthe solvent was evaporated under reduced pressure
  3. additionThe residue was diluted with an ether, diethanolamine (1.25 mL)
  4. additionwas added to the diluent, and the reaction solution
  5. stirringwas stirred at room temperature overnight
  6. filtrationThe reaction solution was filtered on a celite
  7. concentrationthe filtrate was concentrated under reduced pressure
  8. customThe residue was purified by silica gel column chromatography (elution solvent:heptane-ethyl acetate system)

Sources & evidence

ORD record
ord-182d884889e94a60a98c5de05fb9ba4b
Source dataset
uspto-grants-2010_02
Patent number
US07667041B2

Reaction notes

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