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

HRID 38383
Notes
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Reaction equation

HRID 38383 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 176Acetic AcidHCID 8028TetrahydrofuranHCID 8254Dimethyl EtherHCID 8470Trimethyl borateHCID 178418339Butyllithium

Product 1

HCID 225718926-Methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acidYield 98%

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-463a06b6a5744d23874d7f074c135326
Source dataset
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08524725B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes