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Diisobutylaluminum hydride → 4-Bromo-2,6-dimethylbenzaldehyde

HRID 1177405
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HRID 1177405 반응식
CC(C[AlH]CC(C)C)C.[Br:10][C:11]1[CH:18]=[C:17]([CH3:19])[C:14]([C:15]#N)=[C:13]([CH3:20])[CH:12]=1.C(C(C(C([O-])=O)O)O)([O-])=[O:22].[K+].[Na+]>C(Cl)Cl>[Br:10][C:11]1[CH:18]=[C:17]([CH3:19])[C:14]([CH:15]=[O:22])=[C:13]([CH3:20])[CH:12]=1
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참가 물질

5

반응물 3

HCID 14487Diisobutylaluminum hydrideHCID 9855836Potassium sodium tartarateHCID 109107954-Bromo-2,6-dimethylbenzonitrile

생성물 1

HCID 110202224-Bromo-2,6-dimethylbenzaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
25 °C

실험 절차

DIBAL-H (1.0M in hexanes; 22.0 mL, 22.0 mmol) was added to a solution of 4-bromo-2,6-dimethylbenzonitrile (3.87 g, 18 mmol) in CH2Cl2 (50 mL) at 0° C., and the resulting mixture stirred at 25° C. for 3 h. Saturated aqueous sodium potassium tartrate solution (75 mL) was then slowly added, and the resulting mixture was stirred vigorously for 30 min. The organic layer was separated, and the aqueous layer was extracted with CH2Cl2). The combined organic extracts were dried over MgSO4, filtered, and concentrated in vacuo. Chromatographic purification of the residue (silica gel, 0-20% EtOAc/hexanes) furnished 4-bromo-2,6-dimethylbenzaldehyde as a light brown solid.

후처리

  1. stirringthe resulting mixture was stirred vigorously for 30 min
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with CH2Cl2)
  4. dry with materialThe combined organic extracts were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customChromatographic purification of the residue (silica gel, 0-20% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-b07de9ef1e7845448be588a71069844b
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07842685B2

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