반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[C:4]=1/[CH:11]=[CH:12]/[CH:13]=O.[N:15]([CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])=[N+:16]=[N-:17].[Na].[Cl-].[NH4+]>C(O)C.CCO.CCO>[N:15](/[C:18](=[CH:13]/[CH:12]=[CH:11]/[C:4]1[C:5]([O:9][CH3:10])=[CH:6][CH:7]=[CH:8][C:3]=1[O:2][CH3:1])/[C:19]([O:21][CH2:22][CH3:23])=[O:20])=[N+:16]=[N-:17]참가 물질
반응 조건
- 온도
- -10 °C
실험 절차
Add dropwise, while stirring, a solution of 37 g (192 mmol) of (2E)-3-(2,6-dimethoxyphenyl)acrylaldehyde and 85.7 g (664 mmol) of ethyl 2-azidoacetate in 200 mL of absolute ethanol EtOH to a solution of 15.5 g (673 mmol) of sodium in 500 mL of absolute EtOH cooled to −10° C. and kept under argon, maintaining the temperature at −10° C. After stirring at −10° C. for 3 h, stir the reaction mixture for 15 h at RT, then pour into 600 mL of an aqueous solution of ammonium chloride (NH4Cl) at 30 wt. %. After filtration on a frit and rinsing with 2×200 mL of water, take up the precipitate in 600 mL of DCM, dry over Na2SO4 and concentrate under reduced pressure, which leads to 42 g of ethyl (2E,4E)-2-azido-5-(2,6-dimethoxyphenyl)penta-2,4-dienoate in the form of a yellow solid.
후처리
- additionAdd dropwise
- stirringAfter stirring at −10° C. for 3 h
- stirringstir the reaction mixture for 15 h at RT
- filtrationAfter filtration on a frit
- washrinsing with 2×200 mL of water
- dry with materialdry over Na2SO4
- concentrationconcentrate under reduced pressure, which
출처 및 근거
- ORD 기록
- ord-b55a78e8229d448bb0dc1dd34a2ae4b4
- 출처 데이터셋
- uspto-grants-2012_02
- 특허 번호
- US08110579B2
연결된 노트
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