반응식
[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1.[CH3:12][C:13](=[CH:15][CH2:16][CH2:17][C@@H:18]([CH2:20][CH2:21][OH:22])[CH3:19])[CH3:14]>C(Cl)Cl>[CH3:19][C@@H:18]1[CH2:20][C:21](=[O:22])[C:15](=[C:13]([CH3:14])[CH3:12])[CH2:16][CH2:17]1참가 물질
4
실험 절차
10 l of CH2Cl2 and 1704 g (7.89M) of pyridinium chlorochromate were introduced in a four neck reaction vessel equipped with a mechanical stirrer, a thermometer, a condenser and an inlet tube for nitrogen. To this mixture and under nitrogen, 400 g (2.56M) of (-)-(S)-β-citronellol were added while the temperature was kept at 15°-20°. Stirring was then carried on for 60 h at room temperature. After filtration, the mixture was extracted with CH2Cl2 and the combined organic extracts were washed with 15% HCl, saturated NaHCO3, then with water until neutrality. Evaporation and distillation on residue at 7.8 mmHg gave 206.9 g of (-)-pulegone and (-)-isopulegone (40:60) (yield 37%). B.p. 62°/7.8 mmHg).
후처리
- customequipped with a mechanical stirrer
- customwas kept at 15°-20°
- customwas then carried on for 60 h at room temperature
- filtrationAfter filtration
- extractionthe mixture was extracted with CH2Cl2
- washthe combined organic extracts were washed with 15% HCl, saturated NaHCO3
- customEvaporation and distillation on residue at 7.8 mmHg
출처 및 근거
- ORD 기록
- ord-cda117fcf1b74652baf7b2be98c45a20
- 출처 데이터셋
- uspto-grants-1992_01
- 특허 번호
- US05081312
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