Hydrogen Bromide → 3-Methylpiperidin-4-one hydrobromide
반응식
C([N:5]1[CH2:10][CH2:9][C:8](=[O:11])[C:7](C(OC)=O)([CH3:12])[CH2:6]1)(OC)=O.[BrH:17]>CO>[BrH:17].[CH3:12][CH:7]1[C:8](=[O:11])[CH2:9][CH2:10][NH:5][CH2:6]1참가 물질
4
실험 절차
A solution of 1,3-dicarbomethoxy-3-methyl-4-piperidone (51.45 g, 225 mmol) in hydrobromic acid (48%, 250 mL) is heated under reflux for 4 h and then cooled to room temperature. The resultant solution is concentrated in vacuo to give an orange colored solid. The solid is suspended in methanol (50 mL) and concentrated in vacuo again to give 3-methyl-4-piperidone hydrobromide salt: 42.9 g; 98%; mp 203°-205° C.
후처리
- temperatureunder reflux for 4 h
- concentrationThe resultant solution is concentrated in vacuo
- customto give an orange colored solid
- concentrationconcentrated in vacuo again
출처 및 근거
- ORD 기록
- ord-f93e8ecb4d8445cd8f7ec67a6d88decd
- 출처 데이터셋
- uspto-grants-1992_07
- 특허 번호
- US05130321
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