Hydrochloric Acid → 2,3-Methylenedioxyphenyl boronic acid

HRID 602439

Reaction equation

HRID 602439 reaction equation
[Li]CCCC.Br[C:7]1[C:15]2[O:14][CH2:13][O:12][C:11]=2[CH:10]=[CH:9][CH:8]=1.[B:16](OC(C)C)([O:21]C(C)C)[O:17]C(C)C.Cl.[OH-].[Na+]>O1CCCC1>[O:12]1[C:11]2[CH:10]=[CH:9][CH:8]=[C:7]([B:16]([OH:21])[OH:17])[C:15]=2[O:14][CH2:13]1

Participants

7

Procedure

nBuLi (2.5M in hexanes, 2.38 mL, 5.97 mmol) was dropwise added to a solution of 4-bromo-1,3-benzodioxole (1 g, 4.97 mmol) and triisopropyl borate (1.49 mL, 6.47 mmol) in 50 mL of dry tetrahydrofuran at −78° C. under argon. The reaction was maintained at that temperature for 3 hours, then warmed up to room temperature and cooled back to 0° C. immediately. The solution was acidified to pH=2 with HCl 2N and neutralized to pH=7 with NaOH 2N, it was then extracted with ethyl acetate (3×25 ml), the organic solution was washed with brine, dried over sodium sulphate and the solvent removed under reduced pressure to yield the title compound (570 mg, 69%) as a white solid.

Workup

  1. temperatureThe reaction was maintained at that temperature for 3 hours
  2. temperaturecooled back to 0° C. immediately
  3. extractionwas then extracted with ethyl acetate (3×25 ml)
  4. washthe organic solution was washed with brine
  5. dry with materialdried over sodium sulphate
  6. customthe solvent removed under reduced pressure

Sources & evidence

ORD record
ord-47182cfc45854eaabaf89991df4e4618
Source dataset
uspto-grants-2011_03
Patent number
US07906530B2

Linked notes

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