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Water → (2,6-Dimethoxyphenyl)boronic acid

HRID 24630
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HRID 24630 반응식
[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]
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참가 물질

7

반응물 4

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

생성물 1

HCID 2734343(2,6-Dimethoxyphenyl)boronic acid

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 8028
Tetrahydrofuran
용매

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온도
-78 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-d59ade9a59d241b4931c9e0bd6130bdd
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06855843B2

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