Acetic Acid → 6-Methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acid

HRID 2266127

Reaktionsgleichung

Reaktionsgleichung von HRID 2266127
[CH3:1][O:2][CH3:3].[CH2:4]([Li])CCC.[B:9]([O:14]C)([O:12]C)OC.[CH3:16][C:17]([OH:19])=O.[CH2:20]1[CH2:24][O:23][CH2:22][CH2:21]1>>[CH3:1][O:2][C:3]1[CH:4]=[CH:16][C:17]2[O:19][CH2:20][CH2:24][O:23][C:22]=2[C:21]=1[B:9]([OH:12])[OH:14]

Komponenten

6

Versuchsvorschrift

To a solution of methyl ether X (10.0 g, 60 mmol) in 50 ml THF at −78° C. was added n-butyllithium (36 ml, 90 mmol, 2.5 M in hexanes) was added drop-wise. After 1 h the solution was warmed to rt. After 1 h the solution was cooled to −78° C. and trimethyl borate (13.6 ml, 120 mmol) was added. The solution was warmed to rt. After 16 h the mixture was quenched by the addition of water and resulting mixture was acidified with AcOH and extracted with ethyl acetate. The combined organics were washed with saturated NaHCO3, dried with MgSO4, filtered and concentrated in vacuo. The resulting oil was azeotroped with toluene to afford 6-methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acid (13.72 g, 98%) as an oil.

Aufarbeitung

  1. additionwas added drop-wise
  2. temperatureAfter 1 h the solution was cooled to −78° C.
  3. temperatureThe solution was warmed to rt
  4. customAfter 16 h the mixture was quenched by the addition of water
  5. customresulting mixture
  6. extractionextracted with ethyl acetate
  7. washThe combined organics were washed with saturated NaHCO3
  8. dry with materialdried with MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. customThe resulting oil was azeotroped with toluene

Quellen und Nachweise

ORD-Eintrag
ord-a7fd0cf738bd462887f493f5d5fdd0f1
Quelldatensatz
uspto-grants-2010_12
Patentnummer
US07858632B2

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