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2-Bromo-4'-(trifluoromethyl)acetophenone → HCID 22147881, 화합물

HRID 1823886
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HRID 1823886 반응식
[Cl:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1[C:7]([NH2:9])=[O:8].[F:10][C:11]([F:23])([F:22])[C:12]1[CH:21]=[CH:20][C:15]([C:16](=O)[CH2:17]Br)=[CH:14][CH:13]=1>>[Cl:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1[C:7]1[O:8][CH:17]=[C:16]([C:15]2[CH:20]=[CH:21][C:12]([C:11]([F:10])([F:22])[F:23])=[CH:13][CH:14]=2)[N:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 3219792-Bromo-4'-(trifluoromethyl)acetophenoneHCID 28080883-Chloro-2-thiophenecarboxamide

생성물 1

HCID 22147881HCID 22147881, 화합물수율 6%

반응 조건

온도
150 °C

실험 절차

3-Chloro-thiophene-2-carboxamide (0.145 g, 0.898 mmol) and 4-trifluoromethyl-phenacyl bromide (0.200 g, 0.749 mmol) were placed in a sealed tube and heated at 150° C. for 4 h. The reaction mixture was quenched with ethyl acetate and the residue was purified by column chromatography (gradient 100:1, 20:1 hexane:dichloromethane). The product was further purified by preparative-TLC (100:1, hexane:dichloromethane) to yield 0.0148 g (5.0%) of the title compound as a white solid. 1H NMR (Acetone-d6): 8.58 (s, 1H), 8.01 (d, J=8.1 Hz, 2H), 7.71 (t, 3H), 7.10 (d, J=5.1 Hz, 1H), 7.08 (d, J=5.7 Hz, 1H).

후처리

  1. customThe reaction mixture was quenched with ethyl acetate
  2. customthe residue was purified by column chromatography (gradient 100:1, 20:1 hexane:dichloromethane)
  3. customThe product was further purified by preparative-TLC (100:1, hexane:dichloromethane)

출처 및 근거

ORD 기록
ord-83ba85a6efe34ff0898db704961d6d52
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07041685B2

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