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Dimethylformamide → HCID 53645791, 화합물

HRID 1387349
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HRID 1387349 반응식
CN(C)C=O.C(=O)([O-])[O-].[K+].[K+].Cl[C:13]1[CH:18]=[CH:17][C:16]([C:19]([F:22])([F:21])[F:20])=[CH:15][N:14]=1.[CH3:23][O:24][N:25]=[C:26]([C:34]1[O:35][CH2:36][CH2:37][N:38]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[OH:33]>[OH-].[Na+]>[CH3:23][O:24][N:25]=[C:26]([C:34]1[O:35][CH2:36][CH2:37][N:38]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[O:33][C:13]1[CH:18]=[CH:17][C:16]([C:19]([F:22])([F:21])[F:20])=[CH:15][N:14]=1
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참가 물질

6

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HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 923422-Chloro-5-(trifluoromethyl)pyridineHCID 1361714202-hydroxyphenyl 2-oxazolin-2-yl ketone O-methyloxime

생성물 1

HCID 53645791HCID 53645791, 화합물수율 52.1%

시약·촉매·용매 1

HCID 14798
Sodium Hydroxide
용매

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온도
100 °C

실험 절차

N,N-Dimethylformamide (2.2 ml), potassium carbonate (210 mg, 1.5 mmol) and 2-chloro-5-trifluoromethylpyridine (220 mg, 1.2 mmol) were added to 2-hydroxyphenyl 2-oxazolin-2-yl ketone O-methyloxime (220 mg, 1.0 mmol), and the mixture was stirred at 100° C. for 2.5 hours. After completion of the reaction, aqueous in sodiumhydroxide solution (100 ml) was added, and the mixture was extracted with ether. The ether layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give 2-(5-trifluoromethyl-2-pyridyloxy)phenyl 2-oxazolin-2-yl ketone O-methyloxime (190 mg, 52.1%) as an oil.

후처리

  1. customAfter completion of the reaction
  2. extractionthe mixture was extracted with ether
  3. dry with materialThe ether layer was dried over anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel chromatography (ethyl acetate/n-hexane)

출처 및 근거

ORD 기록
ord-148956bb24d241f0abd2753318a91f59
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06268312B1

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