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Dimethylformamide → HCID 19860705, 화합물

HRID 232177
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HRID 232177 반응식
CS([CH2:5][C:6]([F:10])([F:9])[CH:7]=[CH2:8])(=O)=O.[C:11]1([C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][O:13]1)=[O:12].[K].C[N:23](C)C=O>>[C:14]1(=[O:13])[N:23]([CH2:5][C:6]([F:10])([F:9])[CH:7]=[CH2:8])[C:11](=[O:12])[C:20]2=[CH:19][CH:18]=[CH:17][CH:16]=[C:15]12
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참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 19860699HCID 19860699, 화합물HCID 67006573Potassium phthalide

생성물 1

HCID 19860705HCID 19860705, 화합물

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온도
110 °C

실험 절차

The compound 1-methanesulfonyl-2,2-difluoro-3-butene (11.2 g, 60.2 mM), potassium phthalide (12.3 g, 66.4 mM) and dry dimethylformamide (30 mL) are stirred and heated (bath temperature 110° C.) under nitrogen for 120 hours. After cooling to room temperature, the crude reaction product is precipitated by the addition of water (approximately 300 mL), filtered and dissolved in dichloromethane. The dichloromethane solution is washed with 1N potassium hydroxide (twice), water (twice), dried (Na2SO4) and evaporated to yield 1-phthalimido-2,2-difluoro-3-butene as beige-colored crystals: 11.9 g (83%).

후처리

  1. temperatureAfter cooling to room temperature
  2. customthe crude reaction product
  3. customis precipitated by the addition of water (approximately 300 mL)
  4. filtrationfiltered
  5. dissolutiondissolved in dichloromethane
  6. washThe dichloromethane solution is washed with 1N potassium hydroxide (twice), water (twice),
  7. dry with materialdried (Na2SO4)
  8. customevaporated

출처 및 근거

ORD 기록
ord-8334b1fe3d3a4a2188167f45c9f3d520
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04851448

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