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Water → [5-(Propan-2-yl)-1,2-oxazol-3-yl]methanol

HRID 2261332
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HRID 2261332 반응식
[CH:1]([C:4]1[O:8][N:7]=[C:6]([C:9](OCC)=[O:10])[CH:5]=1)([CH3:3])[CH3:2].[BH4-].[Na+].O>C(O)C>[CH:1]([C:4]1[O:8][N:7]=[C:6]([CH2:9][OH:10])[CH:5]=1)([CH3:3])[CH3:2]
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참가 물질

5

반응물 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 18361884Ethyl 5-(propan-2-yl)-1,2-oxazole-3-carboxylate

생성물 1

HCID 25220768[5-(Propan-2-yl)-1,2-oxazol-3-yl]methanol수율 94.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

20.76 g of ethyl 5-i-propyl-isoxazole-3-carboxylate was dissolved in 200 ml of ethanol, and 4.20 g of sodium borohydride was then added. The mixture was stirred at room temperature for 10 hours. After 50 ml of water was added, the reaction mixture was concentrated to 50 ml under reduced pressure. The concentrated solution was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 15.13 g of (5-i-propyl-isoxazol-3-yl)methanol.

후처리

  1. concentrationthe reaction mixture was concentrated to 50 ml under reduced pressure
  2. extractionThe concentrated solution was extracted with ethyl acetate
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-6f969d39433347df94361895b69626cb
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846956B2

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