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Chloroacetone → HCID 11109189, 화합물

HRID 1700627
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HRID 1700627 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[CH2:13][C:12](=[O:14])[CH:11]=[C:10]([SH:15])[CH2:9]1.Cl[CH2:17][C:18](=[O:20])[CH3:19].[O-]CC.[Na+]>C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[CH2:13][C:12](=[O:14])[CH:11]=[C:10]([S:15][CH2:17][C:18](=[O:20])[CH3:19])[CH2:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6571ChloroacetoneHCID 2723922Sodium ethoxideHCID 11118132HCID 11118132, 화합물

생성물 1

HCID 11109189HCID 11109189, 화합물수율 103.5%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

To a solution of 5-(2-chlorophenyl)-3-mercapto-2-cyclohexen-1-one (1.8 g) and chloroacetone (0.7 g) in ethanol (20 ml) was added a solution of 20% sodium ethoxide in ethanol (0.48 g), and the mixture was stirred at room temperature for 5 hours. The reaction solution was concentrated under reduced pressure, and to the residue was ethyl acetate. The mixture was subjected to extraction, and the organic layer was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure to give 5-(2-chlorophenyl)-3-(2-oxopropylthio)-2-cyclohexen-1-one (2.3 g).

후처리

  1. concentrationThe reaction solution was concentrated under reduced pressure
  2. extractionThe mixture was subjected to extraction
  3. washthe organic layer was washed with water and saturated brine
  4. dry with materialdried with magnesium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7f968d3dce3a4174a6da2b85f7f770fb
출처 데이터셋
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06350749B1

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