Hydrochloric Acid → 5-Fluoro-2-methoxyphenylboronic acid

HRID 2290059Notes

Reaction equation

HRID 2290059 reaction equation
Br[C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[O:9][CH3:10].C(=O)=O.CC(O)C.[Li]CCCC.C[O:24][B:25](OC)[O:26]C.Cl.[NH4+].[Cl-]>C1COCC1>[F:8][C:6]1[CH:5]=[CH:4][C:3]([O:9][CH3:10])=[C:2]([B:25]([OH:26])[OH:24])[CH:7]=1

Participants

8

Conditions

Temperature
-78 °C

Procedure

In a 200-mL flask, a solution of 2-bromo-4-fluoroanisole (Aldrich: 4.00 mL, 30.8 mmol) in THF (50 mL) was cooled to -78° C. (CO2 /IPA). To this solution n-BuLi (Aldrich: 2.5 M in hexanes; 12.4 mL, 31 mmol, 1.0 equivuiv) was added dropwise over a 30 min period. The reaction mixture was stirred at -78° C. for 60 min and treated with trimethylborate (Aldrich: 10.5 mL, 92.4 mmol, 3.0 equivuiv). The reaction mixture was allowed to slowly warm to rt, stirred overnight (12h), and cooled to 0° C. (ice/H2O). The solution was treated with 5% HCl until the pH reached 6. The reaction mixture was poured into sat'd NH4Cl (80 mL) and extracted with CH2Cl2 (3×100 mL). The extracts were washed with sat'd NH4Cl (1×80 mL), combined, dried (MgSO4), filtered through a pad of Celite™, and concentrated to afford 4.90 g (94%) of a white semi-solid. Data for 5-fluoro-20methozyphenylboronic acid: 1H NMR (400 MHz, acetone-d6): 7.47 (dd,J=8.8, 3.3, 1H); 7.17 (m, 1H); 7.05 (dd,J=9.0, 3.9, 1H); 3.93 (s, 3H).

Workup

  1. temperatureto slowly warm to rt
  2. extractionextracted with CH2Cl2 (3×100 mL)
  3. washThe extracts were washed with sat'd NH4Cl (1×80 mL)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered through a pad of Celite™
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-e51c020f63cd40d88a1a4211c8450353
Source dataset
uspto-grants-2000_07
Patent number
US06093821

Reaction notes

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