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4-(Trifluoromethyl)aniline → N-[4-(trifluoromethyl)phenyl]-3-oxopentanoic acid amide

HRID 1354536
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HRID 1354536 반응식
[O:1]=[C:2]([CH2:8][CH3:9])[CH2:3][C:4]([O:6]C)=O.[F:10][C:11]([F:20])([F:19])[C:12]1[CH:18]=[CH:17][C:15]([NH2:16])=[CH:14][CH:13]=1>C1(C)C=CC=CC=1>[F:10][C:11]([F:19])([F:20])[C:12]1[CH:13]=[CH:14][C:15]([NH:16][C:4](=[O:6])[CH2:3][C:2](=[O:1])[CH2:8][CH3:9])=[CH:17][CH:18]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 99644-(Trifluoromethyl)anilineHCID 121699Methyl 3-oxovalerate

생성물 1

HCID 11961981N-[4-(trifluoromethyl)phenyl]-3-oxopentanoic acid amide수율 57%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
0 °C

실험 절차

Methyl 3-oxopentanoate 10.0 g (76.8 mmol) was heated to 115° C. and 4-(trifluoromethyl)aniline 12.83 g (79.6 mmol) was added dropwise thereto for 10 minutes. After stirring at the same temperature for 25 minutes, toluene (50 mL) was added and the resulting reaction solution was further heated and stirred for 12 hours. The reaction solution was cooled to 0° C. to precipitate a solid and subjected to vacuum filtration to obtain N-[4-(trifluoromethyl)phenyl]-3-oxopentanoic acid amide as a white solid (11.22 g, isolated yield: 57%). 1H-NMR (CDCl3, 400 MHz/ppm): δ 1.13 (3H, t), 2.64 (2H, q), 3.60 (2H, s), 7.58 (2H, d), 7.69 (2H, d), 9.52 (1H, br)

후처리

  1. customthe resulting reaction solution
  2. temperaturewas further heated
  3. stirringstirred for 12 hours
  4. customto precipitate a solid
  5. filtrationsubjected to vacuum filtration
  6. customto obtain

출처 및 근거

ORD 기록
ord-86a3e9ce5d7e492eac4b3c45458b497b
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07223859B2

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