Carbon tetrabromide → HCID 22279681, 화합물

HRID 1063470노트

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HRID 1063470 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:20]([Br:24])(Br)(Br)[Br:21].[CH:25]1([O:31][CH2:32][CH2:33][CH:34]=O)[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1>ClCCl>[CH:25]1([O:31][CH2:32][CH2:33][CH:34]=[C:20]([Br:24])[Br:21])[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1

참가 물질

5

실험 절차

A dichloromethane solution (120 ml) of triphenylphosphine (57.7 g, 0.22 mol) in an ice bath were added dropwise to the dichloromethane solution (120 ml) including carbon tetrabromide (36.5 g, 0.11 mol) under a nitrogen atmosphere. After the end of dropping, the reaction mixture was stirred for 5 more minutes. To the reaction solution in the ice bath was added dropwise under a nitrogen atmosphere a dichloromethane solution (90 ml) of the crude 3-cyclohexyloxypropionaldehyde (8.6 g) obtained above, and after dropping, the reaction mixture was stirred for 25 more minutes. The reaction solution was diluted with dichloromethane, and washed with a saturated aqueous sodium hydrogencarbonate solution and then with a saturated aqueous sodium chloride solution. After the dichloromethane layer was dried over anhydrous sodium sulfate, the solvent was evaporated in vacuo. The residue was purified by chromatography on a silica gel column (elution solvent; hexane:ethyl acetate=100:1-33:1) to afford 4-cyclohexyloxy-1,1-dibromobut-1-ene (12.6 g, 55% yield, 2 processes).

후처리

  1. customobtained above, and
  2. stirringthe reaction mixture was stirred for 25 more minutes
  3. washwashed with a saturated aqueous sodium hydrogencarbonate solution
  4. dry with materialAfter the dichloromethane layer was dried over anhydrous sodium sulfate
  5. customthe solvent was evaporated in vacuo
  6. customThe residue was purified by chromatography on a silica gel column (elution solvent; hexane:ethyl acetate=100:1-33:1)

출처 및 근거

ORD 기록
ord-2fa8f4c4549c470eb51915b8b62e9558
출처 데이터셋
uspto-grants-2005_11
특허 번호
US06964976B2

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