Water → ETHYL 2-(QUINOLIN-4-YL)ACETATE
반응식
[CH2:1]([O:3][C:4]([CH:6](C(OCC)=O)[C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[N:10]=[CH:9][CH:8]=1)=[O:5])[CH3:2].[Na+].[Cl-].O>CS(C)=O>[CH2:1]([O:3][C:4]([CH2:6][C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[N:10]=[CH:9][CH:8]=1)=[O:5])[CH3:2]참가 물질
반응 조건
- 온도
- 160 °C
실험 절차
4-(Bis-ethoxycarbonyl methyl)-quinoline (5.05 g, 17.6 mmol), NaCl (2.06 g, 35.2 mmol), and H2O (0.63 mL, 35 mmol) were combined with DMSO (22 mL) in a round-bottom flask fitted with a reflux condenser. The heterogeneous mixture was stirred and heated to 160° C. for 90 minutes. TLC analysis (silca, 20% EtOAc-hexanes) indicated complete consumption of the starting material. The reaction was allowed to cool to room temperature and then was diluted with H2O. The dilution was extracted three times with EtOAc. The organic extracts were combined, washed with brine solution, dried over Na2SO4, filtered through celite, and concentrated. Purification by gradient elution chromatography (SiO2, 20% EtOAc-hexanes to 30% EtOAc-hexanes) gave 4-(ethoxycarbonyl methyl)-quinoline (1.81 g, 8.40 mmol) in 48% yield. MS (APCI) m/z 216.1 (M+H). 1H NMR (300 MHz) CDCl3 δ 8.87 (d, J=4.4 Hz, 1H), 8.14 (d, J=8.0 Hz, 1H), 8.00 (d, J=8.4 Hz, 1H), 7.73 (m, 1H), 7.60 (m, 1H), 7.34 (d, J=4.5 Hz, 1H), 4.17 (q, J=7.1 Hz, 2H), 4.07 (s, 2H), 1.23 (t, J=7.2 Hz, 3H).
후처리
- customfitted with a reflux condenser
- customconsumption of the starting material
- temperatureto cool to room temperature
- additionwas diluted with H2O
- extractionThe dilution was extracted three times with EtOAc
- washwashed with brine solution
- dry with materialdried over Na2SO4
- filtrationfiltered through celite
- concentrationconcentrated
- customPurification
- washby gradient elution chromatography (SiO2, 20% EtOAc-hexanes to 30% EtOAc-hexanes)
출처 및 근거
- ORD 기록
- ord-af9d8c5a08ea46649dc4df37d261d6f5
- 출처 데이터셋
- uspto-grants-2005_04
- 특허 번호
- US06875765B2
반응 노트
불러오는 중…