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Trimethyl borate → [2,6-Dimethoxy-4-(1-methoxyethyl)phenyl]boronic acid

HRID 41250
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HRID 41250 반응식
Br[C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([CH:10]([O:12][CH3:13])[CH3:11])=[CH:4][C:3]=1[O:14][CH3:15].C([Li])CCC.[B:21](OC)([O:24]C)[O:22]C.[Cl-].[NH4+]>O1CCCC1>[CH3:15][O:14][C:3]1[CH:4]=[C:5]([CH:10]([O:12][CH3:13])[CH3:11])[CH:6]=[C:7]([O:8][CH3:9])[C:2]=1[B:21]([OH:24])[OH:22]
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참가 물질

6

반응물 4

HCID 8470Trimethyl borateHCID 25517Ammonium ChlorideHCID 582234192-Bromo-1,3-dimethoxy-5-(1-methoxyethyl)benzeneHCID 178418339Butyllithium

생성물 1

HCID 58223453[2,6-Dimethoxy-4-(1-methoxyethyl)phenyl]boronic acid수율 77%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

To a tetrahydrofuran (200 ml) solution of 2-bromo-1,3-dimethoxy-5-(1-methoxyethyl)benzene (7.39 g, 26.9 mmol), was added dropwise 1.57M n-butyl lithium (18.8 ml, 29.6 mmol) at −78° C., and the mixture was stirred for 30 minutes. To the mixture, was added dropwise trimethyl borate (6.00 ml, 53.8 mmol), and warmed to room temperature. After the reaction was completed, a saturated aqueous solution of ammonium chloride was added while cooling on ice, which was extracted with ethyl acetate and dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-heptane/ethyl acetate=1/1) to obtain the title compound (4.97 g, 20.7 mmol)

후처리

  1. temperaturewhile cooling on ice, which
  2. extractionwas extracted with ethyl acetate
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationthe solvent was then distilled off under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (n-heptane/ethyl acetate=1/1)

출처 및 근거

ORD 기록
ord-63ab5f25dd144985a5ddcef1d408e7c9
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08530504B2

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