Dimethylformamide → 1-[gamma-(p-Chlorophenylsulfinyl)-propyl]piperidine hydrochloride
반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH2:10][CH2:11][CH2:12]Cl)=[O:9])=[CH:4][CH:3]=1.[NH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1.C(=O)([O-])[O-].[Na+].[Na+].CN(C)C=O>O.C1C=CC=CC=1>[ClH:1].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH2:10][CH2:11][CH2:12][N:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)=[O:9])=[CH:4][CH:3]=1참가 물질
실험 절차
A mixture of 2.46 g. of 1-(p-chlorophenylsulfinyl)-3-chloropropane, 0.9 g. of piperidine, 0.53 g. of sodium carbonate in 30 ml. of dimethylformamide is heated for 3 hours at a temperature of 80° - 87°C. After the reaction mixture has been cooled, a mixture of benzene and water is added thereto. The aqueous layer is separated and extracted with benzene. The organic layers are combined, washed with water, dried over sodium sulfate and evaporated under reduced pressure. The oily residue is dissolved in ether and treated with ethanolic hydrogen chloride under cooling. The precipitate is collected by filtration and dried to give 1-[γ-(p-chlorophenylsulfinyl)-propyl]piperidine hydrochloride, m.p.: 170° - 174°C. Recrystallization from benzene gives white crystals, m.p.: 176° - 177°C.
후처리
- additionA mixture of 2.46 g
- temperatureAfter the reaction mixture has been cooled
- additionis added
- customThe aqueous layer is separated
- extractionextracted with benzene
- washwashed with water
- dry with materialdried over sodium sulfate
- customevaporated under reduced pressure
- dissolutionThe oily residue is dissolved in ether
- additiontreated with ethanolic hydrogen chloride
- temperatureunder cooling
- filtrationThe precipitate is collected by filtration
- customdried
출처 및 근거
- ORD 기록
- ord-f5ed92738bf044d4bd62b763fa3aba78
- 출처 데이터셋
- uspto-grants-1976_06
- 특허 번호
- US03960873
반응 노트
불러오는 중…