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Ethyl Acetate → Ethyl 3-oxo-3-(4-(trifluoromethyl)thiazol-2-yl)propanoate

HRID 530760
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반응식

HRID 530760 반응식
C(O[C:4]([C:6]1[S:7][CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[N:10]=1)=[O:5])C.[CH3:15][CH2:16][O:17][C:18]([CH3:20])=[O:19].C(O[K])(C)(C)C>C1(C)C=CC=CC=1>[O:5]=[C:4]([C:6]1[S:7][CH:8]=[C:9]([C:11]([F:12])([F:13])[F:14])[N:10]=1)[CH2:20][C:18]([O:17][CH2:16][CH3:15])=[O:19]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8857Ethyl AcetateHCID 23560697Ethyl 4-(trifluoromethyl)thiazole-2-carboxylateHCID 178418922HCID 178418922, 화합물

생성물 1

HCID 68160095Ethyl 3-oxo-3-(4-(trifluoromethyl)thiazol-2-yl)propanoate수율 45%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
100 °C

실험 절차

To a solution of 4-trifluoromethylthiazole-2-carboxylic acid ethylester (8.88 mmol) in toluene (50 mL) were added successively EtOAc (13.32 mmol) and tBuOK (17.76 mmol). The resulting mixture was stirred at 100° C. for 1 hr. The solvent was removed by evaporation and water and Et2O were added. The solution was neutralized with acetic acid. The extract was washed with water and the organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure to give compound 28 as a yellow oil in 45% yield. MS (ESI, EI−): m/z=266 (MH−).

후처리

  1. customThe solvent was removed by evaporation and water and Et2O
  2. additionwere added
  3. washThe extract was washed with water
  4. dry with materialthe organic layer was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-145880d0f7ac4c79a88cda401751ec9f
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353100B2

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