4-Chlorobenzoyl chloride → 5-(p-Chlorobenzoyl)-2-methoxycarbonyl-4-methylthio-1-methylpyrrole
반응식
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][CH:3]=1.[Cl-].[Al+3].[Cl-].[Cl-].[CH3:15][O:16][C:17]([C:19]1[N:20]([CH3:26])[CH:21]=[C:22]([S:24][CH3:25])[CH:23]=1)=[O:18]>C(Cl)Cl>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([C:21]2[N:20]([CH3:26])[C:19]([C:17]([O:16][CH3:15])=[O:18])=[CH:23][C:22]=2[S:24][CH3:25])=[O:7])=[CH:4][CH:3]=1참가 물질
실험 절차
p-Chlorobenzoyl chloride (2.75 ml, 20 mmol), dissolved 20 ml of methylene chloride and 2.6 g (20 mmol) of aluminum chloride are mixed well at room temperature. After about 5 minutes 1.87 g (10 mmole) of 2-methoxycarbonyl-4-methylthio-1-methylpyrrole is added dropwise. The reaction mixture turns immediately into a dark red colored solution. The reaction is stirred for one hour before it is diluted with 75 ml of methylene chloride and extracted with water. The methylene chloride layer is separated, washed sucessively with 25 ml sodium bicarbonate solution and 50 ml of saturated brine, dried over anhydrous sodium sulfate and concentrated to an oil. The oil is crystallized from ethanol to give 1.0 g of 5-(p-chlorobenzoyl)-2-methoxycarbonyl-4-methylthio-1-methylpyrrole.
후처리
- additionare mixed well at room temperature
- extractionextracted with water
- customThe methylene chloride layer is separated
- washwashed sucessively with 25 ml sodium bicarbonate solution and 50 ml of saturated brine
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated to an oil
- customThe oil is crystallized from ethanol
출처 및 근거
- ORD 기록
- ord-233a0f9f588c4c8abfc04824658be01a
- 출처 데이터셋
- uspto-grants-1984_02
- 특허 번호
- US04434175
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