Diiodomethane → HCID 67191093, 화합물

HRID 546346

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HRID 546346 반응식
[CH2:1]([Zn]CC)[CH3:2].[CH3:6]CCCCC.F[C:13](F)(F)[C:14]([OH:16])=[O:15].ICI.C=[C:23]([CH2:37]CC)[CH2:24][CH2:25][CH:26]([C:32]([O:34][CH2:35][CH3:36])=[O:33])C(OCC)=O>ClCCl>[CH2:1]([O:16][C:14]([CH2:13][CH2:6][C:24]1([CH2:25][CH2:26][C:32]([O:34][CH2:35][CH3:36])=[O:33])[CH2:23][CH2:37]1)=[O:15])[CH3:2]

참가 물질

6

실험 절차

24.5 ml (24.5 mmol) of 1.0 M diethyl zinc/hexane solution was added to 30 ml of dichloromethane, and then a solution of 1.89 ml (24.5 mmol) of trifluoroacetic acid in 10 ml of dichloromethane was added with stirring under ice-cooling. The reaction solution was stirred for 20 minutes at the same temperature, then a solution of 1.97 ml (24.5 mmol) of diiodomethane in 10 ml of dichloromethane was added and stirred for 20 minutes, and 1.40 g (6.13 mmol) of a solution of diethyl 4-methyleneheptanedicarboxylate (compound described in J.A.C.S. 107, 13, 3981-3997 (1985)) in 10 ml of dichloromethane was further added. After the reaction solution was stirred for 6 hours at room temperature, ice water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=5:1) to give 1.48 g of the title compound as a brown oil (yield: 99%).

후처리

  1. temperaturecooling
  2. stirringThe reaction solution was stirred for 20 minutes at the same temperature
  3. stirringstirred for 20 minutes
  4. stirringAfter the reaction solution was stirred for 6 hours at room temperature
  5. extractionthe mixture was extracted with ethyl acetate
  6. washThe organic layer was washed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationfollowed by concentration under reduced pressure

출처 및 근거

ORD 기록
ord-bbe61f53495e4983b81bb8c8d9aceb0a
출처 데이터셋
uspto-grants-2011_05
특허 번호
US07935835B2

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