Iodine → 4,4-Difluoro-2-iodocyclohex-2-en-1-one

HRID 337856노트

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HRID 337856 반응식
[F:1][C:2]1([F:9])[CH2:7][CH2:6][C:5](=[O:8])[CH:4]=[CH:3]1.C(=O)([O-])[O-].[K+].[K+].[I:16]I>CN(C1C=CN=CC=1)C.C1COCC1.O>[F:1][C:2]1([F:9])[CH2:7][CH2:6][C:5](=[O:8])[C:4]([I:16])=[CH:3]1

참가 물질

6

실험 절차

To a solution of the 4,4-difluorocyclohex-2-en-1-one (1.0 g, 7.57 mmol) prepared in Example 88b in a THF-water mixed solvent (1:1; 20 mL), potassium carbonate (1.30 g, 9.41 mmol), iodine (2.9 g, 11.4 mmol) and DMAP (0.56 g, 4.58 mmol) were added, and the reaction solution was stirred at room temperature for 30 minutes. The reaction solution was subjected to extraction with ethyl acetate (20 mL). The thus obtained organic layer was washed with an aqueous sodium thiosulfate solution (20 mL) and dried over anhydrous sodium sulfate. After vacuum concentration, the residue was purified with silica gel chromatography (hexane/ethyl acetate=9:1) to yield the title compound (1.46 g, 75%) as a light brown oil.

후처리

  1. extractionThe reaction solution was subjected to extraction with ethyl acetate (20 mL)
  2. washThe thus obtained organic layer was washed with an aqueous sodium thiosulfate solution (20 mL)
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationAfter vacuum concentration
  5. customthe residue was purified with silica gel chromatography (hexane/ethyl acetate=9:1)

출처 및 근거

ORD 기록
ord-547c4213c6b74cfeacd14d029d8c36cc
출처 데이터셋
uspto-grants-2014_11
특허 번호
US08889741B2

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