Toluene → Ethyl 2-cyano-3-(2-methylphenyl)acrylate
반응식
[CH2:1]([O:3][C:4](=[O:8])[CH2:5][C:6]#[N:7])[CH3:2].N1CCCC[CH2:10]1.[C:15]1([CH3:21])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:6]([C:5](=[CH:21][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH3:10])[C:4]([O:3][CH2:1][CH3:2])=[O:8])#[N:7]참가 물질
4
실험 절차
O-Tolylaldehyde (10 g, 83.2 mmol), ethylcyanoacetate (9.4 g, 83.2 mmol), and piperidine (1.1 mL, 11 mmol) were heated in toluene at reflux for 1 hour. The reaction was washed with H2O and brine, dried over MgSO4, and concentrated, with the resulting residue purified by chromatography (10-50% EtOAc, petroleum ether) to give ethyl 2-cyano-3-o-tolylacrylate (10.6 g, 59%).
후처리
- temperatureat reflux for 1 hour
- washThe reaction was washed with H2O and brine
- dry with materialdried over MgSO4
- concentrationconcentrated, with the resulting residue
- custompurified by chromatography (10-50% EtOAc, petroleum ether)
출처 및 근거
- ORD 기록
- ord-7e184a76c6d6429d8f9864109e7b689b
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08629149B2
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