Ammonium Chloride → Ethyl 3-(4-benzyloxy-2-chlorophenyl)-2-azidopropenoate
반응식
[CH2:1]([O:8][C:9]1[CH:16]=[CH:15][C:12]([CH:13]=O)=[C:11]([Cl:17])[CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:18]([OH:21])(=[O:20])[CH3:19].C([N:24]=[N+:25]=[N-:26])C.[O-][CH2:28][CH3:29].[Na+].[Cl-].[NH4+]>C(O)C>[CH2:1]([O:8][C:9]1[CH:16]=[CH:15][C:12]([CH:13]=[C:19]([N:24]=[N+:25]=[N-:26])[C:18]([O:21][CH2:28][CH3:29])=[O:20])=[C:11]([Cl:17])[CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
반응 조건
- 온도
- -10 °C
실험 절차
An ethanol solution, 70 ml, containing 5.40 g (21.9 mmol) of 4-benzyloxy-2-chlorobenzaldehyde and 11.3 g (87.6 mmol) of ethyl azide acetate was gradually added dropwise to 70 ml of an ethanol solution of 5.95 g (87.6 mmol) of sodium ethoxide at −10° C. After stirring at −10° C. for further 5 hours, the reaction temperature was slowly elevated to room temperature. The reaction mixture was poured onto 200 ml of saturated ammonium chloride aqueous solution and the mixture was extracted three times with ethyl acetate. The combined extracts were then washed with saturated ammonium chloride solution and next with saturated sodium chloride solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography to give 4.50 g (57.5%) of ethyl 3-(4-benzyloxy-2-chlorophenyl)-2-azidopropenoate.
후처리
- customwas slowly elevated to room temperature
- extractionthe mixture was extracted three times with ethyl acetate
- washThe combined extracts were then washed with saturated ammonium chloride solution and next with saturated sodium chloride solution
- dry with materialAfter drying over anhydrous magnesium sulfate
- distillationthe solvent was distilled off under reduced pressure
- customThe resulting residue was purified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-b3ea862860d84752a5790b0c1a26c079
- 출처 데이터셋
- uspto-grants-2001_01
- 특허 번호
- US06169107A
반응 노트
불러오는 중…