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Hydride → (R)-2-[(tert-Butyldimethylsilyl)oxy]-2-(3-chlorophenyl)acetaldehyde

HRID 1004073
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HRID 1004073 반응식
C[O:2][C:3](=O)[C@@H:4]([C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[CH:14]=1)[O:5][Si:6]([C:9]([CH3:12])([CH3:11])[CH3:10])([CH3:8])[CH3:7].[H-]>CCOCC.C1(C)C=CC=CC=1>[Cl:19][C:15]1[CH:14]=[C:13]([C@@H:4]([O:5][Si:6]([C:9]([CH3:12])([CH3:11])[CH3:10])([CH3:7])[CH3:8])[CH:3]=[O:2])[CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 166653HydrideHCID 54113343Methyl (R)-2-[(tert-butyldimethylsilyl)oxy]-2-(3-chlorophenyl)acetate

생성물 1

HCID 11129841(R)-2-[(tert-Butyldimethylsilyl)oxy]-2-(3-chlorophenyl)acetaldehyde수율 85.7%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 3283Diethyl Ether용매

실험 절차

To a stirred solution of (R)-(3-chloro-phenyl)-(tert-butyl-dimethyl-silanoxy)-acetic acid methyl ester (4.0 g) in anhydrous ether (10 ml) and maintained at <-65° was added dropwise a 1.5M solution of di-isobututylaluminium hydride in toluene (10 ml). When addition was complete the solution was stirred at -65° for a further hour, then quenched with methanol (10 ml). The mixture was allowed to attain room temperature when silica (20 g) was added. Solvent was removed under reduced pressure, and the residue was purified by flash chromatography, eluting with cyclohexane:ethyl acetate (9:1) to give the title compound as a colourless liquid (3.1 g).

후처리

  1. additionWhen addition
  2. customquenched with methanol (10 ml)
  3. customto attain room temperature
  4. additionwas added
  5. customSolvent was removed under reduced pressure
  6. customthe residue was purified by flash chromatography
  7. washeluting with cyclohexane:ethyl acetate (9:1)

출처 및 근거

ORD 기록
ord-fc4c706520c747848a8fe1c9ff40bd58
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06048872

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