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Dimethylformamide → HCID 53645791、化合物

HRID 1387349
ノート
印刷プレビュー

反応式

HRID 1387349 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

HCID 53645791HCID 53645791、化合物収率 52.1%

試薬・触媒・溶媒 1

HCID 14798
Sodium Hydroxide
溶媒

反応条件

温度
100 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-148956bb24d241f0abd2753318a91f59
出典データセット
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06268312B1

反応ノート

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