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Water → (2,6-Dimethoxyphenyl)boronic acid

HRID 24630
ノート
印刷プレビュー

反応式

HRID 24630 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[CH:4]=1.[Li]CCCC.[B:16](OC)([O:19]C)[O:17]C.O>C1COCC1.C(O)(=O)C>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[C:4]=1[B:16]([OH:19])[OH:17]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 8470Trimethyl borateHCID 90251,3-DimethoxybenzeneHCID 178418339Butyllithium

生成物 1

HCID 2734343(2,6-Dimethoxyphenyl)boronic acid

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
-78 °C

実験手順

1,3-Dimethoxybenzene (4 g) was dissolved in freshly distilled THF (10 mL). This solution was cooled to −78° C. and n-BuLi (24 mL, 1.6 M solution in hexanes) was added dropwise to the cold solution. The mixture was stirred at −78° C. for 1 h, then warmed to room temperature and stirred for 1 h. The resulting mixture was cooled again to −78° C. and (MeO)3B (6.7 mL) was added. The mixture was allowed to warm to room temperature and stirred overnight. Water (10 mL) was added, and the mixture was stirred for 0.5 h, acidified to pH 4 with acetic acid and extracted with EtOAc. The extract was dried (MgSO4) and evaporated to give 2,6-dimethoxybenzeneboronic acid, which was used without further purification.

後処理

  1. temperaturewarmed to room temperature
  2. stirringstirred for 1 h
  3. temperatureThe resulting mixture was cooled again to −78° C.
  4. temperatureto warm to room temperature
  5. stirringstirred overnight
  6. stirringthe mixture was stirred for 0.5 h
  7. extractionextracted with EtOAc
  8. dry with materialThe extract was dried (MgSO4)
  9. customevaporated

出典と根拠

ORDレコード
ord-d59ade9a59d241b4931c9e0bd6130bdd
出典データセット
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06855843B2

反応ノート

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