반응식
Br.[CH3:2][N:3]1[CH2:12][CH2:11][CH:10]=[C:5]([C:6]([O:8][CH3:9])=[O:7])[CH2:4]1.[Cl-].[Na+].C(=O)([O-])[O-].[Na+].[Na+]>O>[CH3:2][N:3]1[CH2:12][CH2:11][CH:10]=[C:5]([C:6]([O:8][CH3:9])=[O:7])[CH2:4]1참가 물질
5
실험 절차
Methyl 1,2,5,6-tetrahydro-1-methylnicotinate hydrobromide (Arecoline HBr) weighing 350 g, was dissolved in 600 ml of water. To this solution 50 g of sodium chloride was added and allowed to dissolve. To this solution approximately 400 ml of saturated sodium carbonate solution was added and the mixture extracted four times with (4×) 500 ml of ether. The combined ether extracts were dried over sodium sulfate and the ether evaporated under reduced pressure using a 40° water bath. The methyl 1,2,5,6-tetrahydro-1-methylnicotinate was distilled under aspirator vacuum to give 188 g (82%) of a pale yellow liquid with b.p. 85°/20 mm (pressure approximate). The free base was stored in a freezer.
후처리
- dissolutionto dissolve
- extractionthe mixture extracted four times with (4×) 500 ml of ether
- dry with materialThe combined ether extracts were dried over sodium sulfate
- customthe ether evaporated under reduced pressure
- customusing a 40°
- distillationThe methyl 1,2,5,6-tetrahydro-1-methylnicotinate was distilled under aspirator vacuum
출처 및 근거
- ORD 기록
- ord-254aba9788f346829f5343485da1ae8f
- 출처 데이터셋
- uspto-grants-1984_11
- 특허 번호
- US04483990
연결된 노트
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