Dimethylformamide → Dimethyl Quinoline-2,3-dicarboxylate
반응식
[CH3:1]N(C)C=O.P(Cl)(Cl)(Cl)=O.[C:11]1([NH:17][C:18]([C:24]([O:26][CH3:27])=[O:25])=[CH:19][C:20]([O:22][CH3:23])=[O:21])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C(Cl)CCl>[CH3:27][O:26][C:24]([C:18]1[C:19]([C:20]([O:22][CH3:23])=[O:21])=[CH:1][C:12]2[C:11](=[CH:16][CH:15]=[CH:14][CH:13]=2)[N:17]=1)=[O:25]참가 물질
실험 절차
To a solution of dimethylformamide (DMF, 0.10 mol) in ethylene dichloride (EDC, 100 mL), cooled in an ice bath, is added dropwise with stirring phosphorous oxychloride (POCl3, 0.10 mol). The resulting solution is stirred for one and one-half hours at room temperature and then cooled in an ice bath. To the cooled solution is then added, in small increments, a solution of dimethyl 3-phenylaminobut-2-ene-dioate (0.10 mol) in ethylene dichloride. The resulting mixture is thereafter heated to reflux for three hours, cooled, and washed with half saturated brine. The organic phase is washed with half saturated brine. The organic phase is separated from the aqueous phase and dried. The solvent is removed under vaccum, and the residue recrystallized from methanol to afford 18.2 g (0.74 mol) of dimethyl-2,3-quinolinedicarboxylate, mp 105°-106.5° C.
후처리
- temperaturecooled in an ice bath
- additionTo the cooled solution is then added, in small increments
- temperatureThe resulting mixture is thereafter heated
- temperatureto reflux for three hours
- temperaturecooled
- washwashed with half saturated brine
- washThe organic phase is washed with half saturated brine
- customThe organic phase is separated from the aqueous phase
- customdried
- customThe solvent is removed under vaccum
- customthe residue recrystallized from methanol
출처 및 근거
- ORD 기록
- ord-de5bf2a8dd014432b2c69d428e729c4d
- 출처 데이터셋
- uspto-grants-1987_04
- 특허 번호
- US04656283
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