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Isopropanol → Methyl 5-bromo-2-oxopentanoate

HRID 1905671
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HRID 1905671 반응식
CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.[Br:14][CH2:15][CH2:16][CH2:17][CH:18]([OH:23])[C:19]([O:21][CH3:22])=[O:20].C(O)(C)C>CC(C)=O.O>[Br:14][CH2:15][CH2:16][CH2:17][C:18](=[O:23])[C:19]([O:21][CH3:22])=[O:20]
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참가 물질

6

반응물 3

HCID 3776IsopropanolHCID 13769948Methyl 5-bromo-2-hydroxypentanoateHCID 131709961Jones' reagent

생성물 1

HCID 13769949Methyl 5-bromo-2-oxopentanoate수율 92%

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매

실험 절차

Jones' reagent (CrO3 : 9.58 g, H2SO4 : 8.47 ml, H2O: 36.8 ml) was added to a magnetically stirred solution of Part (3) compound (12.53 g, 59.3 mmole) in acetone (150 ml) at room temperature. The addition was controlled to maintain the temperature below 35° C. After the completion of the addition, the reaction was stirred at room temperature for 45 minutes. Isopropyl alcohol (30 ml) was added dropwise and stirred for 30 minutes. The reaction was then diluted with H2O (500 ml) and the products were extracted with CH2Cl2 (1 l.). The CH2Cl2 layer was washed with brine (100 ml×3) and dried over MgSO4. Filtration and evaporation of solvents gave the title compound (11.4 g, 54.5 mmole, 92%) as a colorless liquid.

후처리

  1. additionThe addition
  2. temperatureto maintain the temperature below 35° C
  3. additionAfter the completion of the addition
  4. stirringstirred for 30 minutes
  5. extractionthe products were extracted with CH2Cl2 (1 l.)
  6. washThe CH2Cl2 layer was washed with brine (100 ml×3)
  7. dry with materialdried over MgSO4
  8. filtrationFiltration and evaporation of solvents

출처 및 근거

ORD 기록
ord-a6243fdd763d4e93800122d0d528c111
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04647573

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