HCl butanone → HCID 67152368, 화합물
반응식
O1[C:5]2([CH2:9][CH2:8][N:7]([C@H:10]3[CH2:15][CH2:14][CH2:13][CH2:12][C@@H:11]3[O:16][CH2:17][CH:18]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:6]2)[O:4]CC1.[ClH:31].CC(=O)CC>>[ClH:31].[O:4]=[C:5]1[CH2:9][CH2:8][N:7]([C@H:10]2[CH2:15][CH2:14][CH2:13][CH2:12][C@@H:11]2[O:16][CH2:17][CH:18]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH2:6]1참가 물질
실험 절차
A mixture of (1R,2R)/(1S,2S)-2-(1,4-dioxa-7-azaspiro[4.4]non-7-yl)-1-(2,2-diphenylethoxy)cyclohexane (1.55 g, 3.8 mmol) in 6M HCl-butanone (1:4, v/v, 50 mL) was refluxed for 2 hours. The butanone was evaporated in vacuo and the residue was taken up with water (50 mL). The aqueous solution was extracted with diethyl ether (2×50 mL); the aqueous layer was collected and extracted with dichloromethane (2×50 mL). The combined dichloromethane extracts were dried over sodium sulfate and concentrated in vacuo to yield the crude title compound. The product was crystallized by triturating in diethyl ether and reprecipitated from a mixture of dichloromethane-diethyl ether to yield 1.21 g (80% yield) of the title compound, having the elemental analysis indicated in Table 1.
후처리
- temperaturewas refluxed for 2 hours
- customThe butanone was evaporated in vacuo
- extractionThe aqueous solution was extracted with diethyl ether (2×50 mL)
- customthe aqueous layer was collected
- extractionextracted with dichloromethane (2×50 mL)
- dry with materialThe combined dichloromethane extracts were dried over sodium sulfate
- concentrationconcentrated in vacuo
- customto yield the crude title compound
- customThe product was crystallized
- customby triturating in diethyl ether
- customreprecipitated from a mixture of dichloromethane-diethyl ether
출처 및 근거
- ORD 기록
- ord-ccb26d698f0f409db49e525b6967c34f
- 출처 데이터셋
- uspto-grants-2011_08
- 특허 번호
- US08008342B2
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