Trimethyl borate → 5-Ethyl-2-fluorophenol

HRID 2105011Notes

Reaction equation

HRID 2105011 reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][CH:4]=1)[CH3:2].CN(CCN(CCN(C)C)C)C.[Li]CCCC.B(OC)(OC)[O:28]C>C1COCC1>[CH2:1]([C:3]1[CH:4]=[CH:5][C:6]([F:9])=[C:7]([OH:28])[CH:8]=1)[CH3:2]

Participants

6

Conditions

Temperature
-60 °C

Procedure

To a solution of 1-ethyl-4-fluorobenzene (5.0 g, 40.3 mmol) and PMDTA (8.5 mL, 40.7 mmol) in 20 mL THF at −40° C., was added BuLi (1.4 M in hexanes, 31.6 mL, 44.3 mmol). The tan suspension was stirred at −60° C. for 40 min, was recooled to −78° C., then B(OMe)3 (9.03 mL, 80.6 mmol). The mixture was stirred at −78° C. for 30 min, then was allowed to warm to rt. The reaction was quenched with 8 mL AcOH, then was cooled to 0° C. and treated with 9.8 mL 30% H2O2. The mixture was stirred for 30 min, then was quenched with aq. Na2SO3. The mixture was diluted with hexanes, washed with H2O (3×) and brine, dried (Na2SO4), filtered through 2″ silica gel (eluting with 20% EtOAc/hexanes), then concentrated to afford 5.42 g of Intermediate 188.1 as a pale yellow oil.

Workup

  1. customwas recooled to −78° C.
  2. stirringThe mixture was stirred at −78° C. for 30 min
  3. temperatureto warm to rt
  4. customThe reaction was quenched with 8 mL AcOH
  5. temperaturewas cooled to 0° C.
  6. additiontreated with 9.8 mL 30% H2O2
  7. stirringThe mixture was stirred for 30 min
  8. customwas quenched with aq. Na2SO3
  9. additionThe mixture was diluted with hexanes
  10. washwashed with H2O (3×) and brine
  11. dry with materialdried (Na2SO4)
  12. filtrationfiltered through 2″ silica gel (eluting with 20% EtOAc/hexanes)
  13. concentrationconcentrated

Sources & evidence

ORD record
ord-c79307dd12ee4f2ba72a684b19c7e07d
Source dataset
uspto-grants-2009_08
Patent number
US07576098B2

Reaction notes

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