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HCID 4327531, 화합물 → 2-[4-(Trifluoromethyl)phenyl]-4-isopropyloxazole-5(4H)-one

HRID 490728
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HRID 490728 반응식
C[O:2][C:3](=[O:21])[CH:4]([NH:8][C:9](=O)[C:10]1[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][CH:11]=1)[CH:5]([CH3:7])[CH3:6]>C(OC(=O)C)(=O)C>[CH:5]([CH:4]1[C:3](=[O:2])[O:21][C:9]([C:10]2[CH:11]=[CH:12][C:13]([C:16]([F:17])([F:18])[F:19])=[CH:14][CH:15]=2)=[N:8]1)([CH3:6])[CH3:7]
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3

반응물 1

HCID 4327531HCID 4327531, 화합물

생성물 1

HCID 451231892-[4-(Trifluoromethyl)phenyl]-4-isopropyloxazole-5(4H)-one

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

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온도
95 °C

실험 절차

3-Methyl-2-(4-trifluoromethyl-benzoylamino)-butyric acid methyl ester (4.75 g, 16.42 mmol) is dissolved in acetic anhydride (25 mL) and heated to 95° C. for 3 hr. The mixture is concentrated in vacuo and the residue is partitioned between aqueous saturated sodium hydrogen carbonate (100 mL) and ethyl acetate (100 mL) the layers are separated, the organic phase is washed with water and brine (100 mL each), dried over anhydrous magnesium sulfate, filtered, concentrated in vacuo, and purified over silica gel eluting with 9:1 hexanes:ethyl acetate to afford 4-Isopropyl-2-(4-trifluoromethyl-phenyl)-4H-oxazol-5-one as a colorless oil which solidifies to a white crystalline solid on standing, 4.14 g, 93%. MS (M++1) 272.

후처리

  1. concentrationThe mixture is concentrated in vacuo
  2. customthe residue is partitioned between aqueous saturated sodium hydrogen carbonate (100 mL) and ethyl acetate (100 mL) the layers
  3. customare separated
  4. washthe organic phase is washed with water and brine (100 mL each)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. custompurified over silica gel eluting with 9:1 hexanes

출처 및 근거

ORD 기록
ord-72372ff2ab52492e8dd990c02f6755a3
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07528160B2

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