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Ethanol → Ethyl 2-(3-methylisoxazol-5-yl)acetate

HRID 2401425
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HRID 2401425 반응식
[CH3:1][C:2]1[CH:6]=[C:5]([CH2:7][C:8]([OH:10])=[O:9])[O:4][N:3]=1.[CH3:11][CH2:12]O.OS(O)(=O)=O>>[CH3:1][C:2]1[CH:6]=[C:5]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[O:4][N:3]=1
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참가 물질

4

반응물 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 41955322-(3-Methyl-1,2-oxazol-5-yl)acetic acid

생성물 1

HCID 11593502Ethyl 2-(3-methylisoxazol-5-yl)acetate수율 97.3%

실험 절차

To a solution of 2-(3-methylisoxazol-5-yl)acetic acid (7.28 g, 51.6 mmol) in EtOH (200 mL, 3425 mmol) was added concentrated H2SO4 (0.30 mL, 5.63 mmol) at room temperature. After 48 h, the reaction mixture was concentrated in vacuo to give a dark brown oil. The crude ester was filtered over a plug of silica (50 g) and the product was eluted with 40% Et2O:60% Hexanes (400 mL). The filtrate was subsequently concentrated to give the product ethyl 2-(3-methylisoxazol-5-yl)acetate (8.50 g, 50.2 mmol, 97% yield) as a clear oil. LC/MS m/z 170 [M+H]+.

후처리

  1. concentrationthe reaction mixture was concentrated in vacuo
  2. customto give a dark brown oil
  3. filtrationThe crude ester was filtered over a plug of silica (50 g)
  4. washthe product was eluted with 40% Et2O
  5. concentrationThe filtrate was subsequently concentrated

출처 및 근거

ORD 기록
ord-a6e7ca9cd3bf41e0b6101287b4fdc531
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08796261B2

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