Water → 2-[4-(Trifluoromethyl)phenyl]oxirane

HRID 1506144

反応式

HRID 1506144 の反応式
[I-].C[S+](C)C.[H-].[Na+].[F:8][C:9]([F:19])([F:18])[C:10]1[CH:17]=[CH:16][C:13]([CH:14]=[CH2:15])=[CH:12][CH:11]=1.[OH2:20]>CS(C)=O>[F:8][C:9]([F:18])([F:19])[C:10]1[CH:17]=[CH:16][C:13]([CH:14]2[CH2:15][O:20]2)=[CH:12][CH:11]=1

参加物

6

反応物 4

HCID 962WaterHCID 24758Sodium hydrideHCID 75127Trimethylsulfonium iodideHCID 27827981-Ethenyl-4-(trifluoromethyl)benzene

生成物 1

HCID 99900162-[4-(Trifluoromethyl)phenyl]oxirane収率 81%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒2 回

実験手順

Trimethylsulfonium iodide (4.08 g, 20.0 mmol) in dimethyl sulfoxide (15 mL) was stirred with sodium hydride (55 wt % dispersion in mineral oil, 873 mg, 20.0 mmol) at room temperature for 1 hour and then with 4-(trifluoromethyl)styrene (2.96 g, 17.0 mmol) in dimethyl sulfoxide (10 mL) at room temperature for 2 hours. After addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1 (v/v)) to give the title compound as a colorless oil (2.59 g, yield 81%).

後処理

  1. extractionthe reaction mixture was extracted with ethyl acetate
  2. dry with materialthe organic layer was dried over anhydrous sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1 (v/v))

出典と根拠

ORDレコード
ord-f886d7f436004bc58563b288f1ce0f26
出典データセット
uspto-grants-2015_12
特許番号
US09216999B2

関連ノート

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