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

HRID 41250
ノート
印刷プレビュー

反応式

HRID 41250 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

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)

後処理

  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)

出典と根拠

ORDレコード
ord-63ab5f25dd144985a5ddcef1d408e7c9
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08530504B2

反応ノート

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