Aziridine → HCID 21428810, 화합물
반응식
[NH:1]1[CH2:3][CH2:2]1.C(=O)([O-])O.[Na+].[F:9][C:10]1[CH:18]=[CH:17][C:13]([C:14](Cl)=[O:15])=[C:12]([O:19][CH3:20])[CH:11]=1.[OH-].[Na+]>O.ClC(Cl)Cl>[F:9][C:10]1[CH:18]=[CH:17][C:13]([C:14]([N:1]2[CH2:3][CH2:2]2)=[O:15])=[C:12]([O:19][CH3:20])[CH:11]=1참가 물질
7
반응 조건
- 온도
- 0 °C
실험 절차
To 231 parts of a aziridine solution 0.95M in water are added 16 parts of sodium hydrogen carbonate while stirring vigorously at 0° C. Then there is added dropwise, during a 45 minutes-period, a solution of 36 parts of 4-fluoro-2-methoxybenzoyl chloride in 150 parts of trichloromethane while still cooling at 0° C. Upon completion, stirring is continued for 30-45 minutes without cooling. The reaction mixture is adjusted to pH 8 with a diluted sodium hydroxide solution and the product is extracted three times with trichloromethane. The combined extracts are washed three times with water, dried, filtered and evaporated, yielding 40.5 parts of 1-(4-fluoro-2-methoxybenzoyl)-aziridine as a residue.
후처리
- additionThen there is added dropwise, during a 45 minutes-period
- stirringUpon completion, stirring
- temperaturewithout cooling
- extractionthe product is extracted three times with trichloromethane
- washThe combined extracts are washed three times with water
- customdried
- filtrationfiltered
- customevaporated
출처 및 근거
- ORD 기록
- ord-054f5abc254d43959ea04fcb7d96981f
- 출처 데이터셋
- uspto-grants-1977_06
- 특허 번호
- US04031226
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