Hydrochloric Acid → 4-(Difluoromethoxy)benzeneboronic acid

HRID 550032Notes

Reaction equation

HRID 550032 reaction equation
Br[C:2]1[CH:11]=[CH:10][C:5]([O:6][CH:7]([F:9])[F:8])=[CH:4][CH:3]=1.[B:12](OC(C)C)([O:17]C(C)C)[O:13]C(C)C.C([Li])CCC.Cl>O1CCCC1>[F:8][CH:7]([F:9])[O:6][C:5]1[CH:10]=[CH:11][C:2]([B:12]([OH:17])[OH:13])=[CH:3][CH:4]=1

Participants

6

Procedure

A solution of (4-bromophenoxy)difluoromethane (3 g) and triisopropyl borate (3.42 ml) in tetrahydrofuran (15 ml) was cooled to −78° C. under argon atmosphere, and thereto was added a solution of n-butyl lithium (1.59M hexane solution, 3.42 ml). The mixture was stirred at room temperature overnight. Added thereto was 6N aqueous hydrochloric acid at 0° C., and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was triturated with cold hexane to give 4-(difluoromethoxy)phenylboronic acid (1.88 g) as colorless solid.

Workup

  1. additionAdded
  2. customat 0° C.
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe extract was washed with brine
  5. dry with materialdried over magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure
  7. customthe residue was triturated with cold hexane

Sources & evidence

ORD record
ord-c18061a2d132485eb145d6814e5d82ab
Source dataset
uspto-grants-2011_05
Patent number
US07943788B2

Reaction notes

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