반응식
N([O-])=O.[Na+].N[C:6]1[CH:25]=[CH:24][C:9]([O:10][C:11]2([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH2:16][CH2:15][N:14]([CH3:17])[CH2:13][CH2:12]2)=[CH:8][CH:7]=1.[PH2](O)=O.[OH-].[Na+]>O.Cl>[CH3:17][N:14]1[CH2:15][CH2:16][C:11]([O:10][C:9]2[CH:24]=[CH:25][CH:6]=[CH:7][CH:8]=2)([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:12][CH2:13]1참가 물질
반응 조건
- 온도
- -5 °C
실험 절차
A solution of 3.0 g of sodium nitrite in 18 ml of water is added dropwise to a solution of 10.0 g of 4-(4-aminophenoxy)-1-methyl-4-phenylpiperidine in 12 ml of concentrated hydrochloric acid and 30 ml of water at -10° C. The mixture is subsequently stirred at -5° C. for 45 minutes, 50 ml of 50% strength hypophosphorous acid are added dropwise at -5° C., and the reaction mixture is left to stand at 0° C. for 24 hours. It is rendered alkaline with 6 N sodium hydroxide solution, while cooling with ice, and extracted with diethyl ether. After treating the organic phase with active charcoal, it is dried over sodium sulfate and concentrated. Resulting residue yields (after recrystallization from 100 ml of n-hexane) 5.5 g of the title compound of m.p. 99° to 101° C.
후처리
- waitthe reaction mixture is left
- waitto stand at 0° C. for 24 hours
- temperaturewhile cooling with ice
- extractionextracted with diethyl ether
- additionAfter treating the organic phase with active charcoal, it
- dry with materialis dried over sodium sulfate
- concentrationconcentrated
- customResulting residue yields
- custom(after recrystallization from 100 ml of n-hexane) 5.5 g of the title compound of m.p. 99° to 101° C.
출처 및 근거
- ORD 기록
- ord-273e84636d54429ab569ae05df80628b
- 출처 데이터셋
- uspto-grants-1982_06
- 특허 번호
- US04333942
연결된 노트
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