Acetone → HCID 66931861, 화합물
반응식
[BH4-].[Na+].[CH2:3]1[CH2:25][O:24][C:5]2([CH2:22][CH2:21][C:20]3[C:19]4[C@H:10]([C@H:11]5[C@@:15]([CH2:17][CH:18]=4)([CH3:16])[C:14](=[O:23])[CH2:13][CH2:12]5)[CH2:9][CH2:8][C:7]=3[CH2:6]2)[O:4]1.CC(C)=O.[Cl-].[Na+]>[OH-].[Na+].CO.C(OCC)(=O)C.O>[CH2:25]1[CH2:3][O:4][C:5]2([CH2:22][CH2:21][C:20]3[C:19]4[C@H:10]([C@H:11]5[C@@:15]([CH2:17][CH:18]=4)([CH3:16])[CH:14]([OH:23])[CH2:13][CH2:12]5)[CH2:9][CH2:8][C:7]=3[CH2:6]2)[O:24]1참가 물질
반응 조건
- 온도
- 2 °C
실험 절차
Sodium borohydride (MW=37.8; 18.9 g; 500 mmol) in solution in 0.5 N sodium hydroxide (100 ml) is introduced, over approximately 5 min at around 2° C., into a suspension of 3,3-ethylenedioxyestra-5(10), 9(11)-dien-17-one (MW=314.4; 100 g; 318 mmol) in methanol (1 liter). The mixture is stirred for 2 h at around 2° C. and then acetone (100 ml) is introduced over approximately 15 min at around 5° C. The mixture is stirred for 1 h and the medium is run, at around 20° C., into a stirred mixture of water (2 liters), sodium chloride (500 g) and ethyl acetate (400 ml). The mixture is separated by settling out and the aqueous phase is re-extracted with ethyl acetate. The combined organic phases are washed with water, dried over sodium sulfate and concentrated at normal pressure to 500 ml. The distillation is continued while maintaining the volume constant by gradual introduction of 1,2-dimethoxyethane (DME). The temperature at the end of exchange is 83° C. The solution is used as it is in the subsequent stage, but a dry extract results in the expected product (resin). C20H28O3; MW=316.4:
후처리
- stirringThe mixture is stirred for 1 h
- customThe mixture is separated
- extractionthe aqueous phase is re-extracted with ethyl acetate
- washThe combined organic phases are washed with water
- dry with materialdried over sodium sulfate
- concentrationconcentrated at normal pressure to 500 ml
- distillationThe distillation
- temperaturewhile maintaining the volume constant by gradual introduction of 1,2-dimethoxyethane (DME)
- customis 83° C
- extractiona dry extract
출처 및 근거
- ORD 기록
- ord-dfdaaec6bcf740a796cb532f5b622020
- 출처 데이터셋
- uspto-grants-2008_11
- 특허 번호
- US07449572B2
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