Carbon tetrabromide → HCID 22731440, 화합물
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[C:1]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([S:15]([C:18]1[C:23]([CH3:24])=[CH:22][C:21]([CH3:25])=[CH:20][C:19]=1[CH3:26])(=[O:17])=[O:16])[CH:10]=[C:9]2[CH3:27])(OCC)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(Br)(Br)(Br)[Br:54]>C1COCC1.C(OCC)(=O)C>[Br:54][CH2:1][C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([S:15]([C:18]1[C:23]([CH3:24])=[CH:22][C:21]([CH3:25])=[CH:20][C:19]=1[CH3:26])(=[O:17])=[O:16])[CH:10]=[C:9]2[CH3:27]참가 물질
실험 절차
Under cooling with ice, 5-carboethoxy-3-methyl-1-(2,4,6-trimethylbenzenesulfonyl)indole (1.13 g, 2.94 mmol) was added to a solution of lithium aluminum hydride (223 mg, 5.88 mmol) in THF (10 ml), followed by stirring for 1 hour. The reaction mixture was mixed with ethyl acetate and a 2N aqueous HCl solution and extracted with chloroform. The organic layer was washed with water and saturated brine, dried over magnesium sulfate and evaporated to remove the solvent. The thus obtained residue was dissolved in methylene chloride (20 ml) and mixed with triphenylphosphine (1.06 g, 4.04 mmol) and carbon tetrabromide (1.34 g, 4.04 mmol) under cooling with ice, followed by stirring for 1 hour. The reaction mixture was evaporated to remove the solvent; the thus obtained residue was subjected to silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:5) to give the titled compound (1.12 g, 94%).
후처리
- extractiona 2N aqueous HCl solution and extracted with chloroform
- washThe organic layer was washed with water and saturated brine
- dry with materialdried over magnesium sulfate
- customevaporated
- customto remove the solvent
- dissolutionThe thus obtained residue was dissolved in methylene chloride (20 ml)
- temperatureunder cooling with ice
- stirringby stirring for 1 hour
- customThe reaction mixture was evaporated
- customto remove the solvent
출처 및 근거
- ORD 기록
- ord-62a9a3be3b42444690d5818376f8196c
- 출처 데이터셋
- uspto-grants-2004_04
- 특허 번호
- US06720433B2
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