HCl butanone → HCID 67152368、化合物
反応式
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]1参加物
実験手順
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.
後処理
- 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
出典と根拠
- ORDレコード
- ord-ccb26d698f0f409db49e525b6967c34f
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US08008342B2
反応ノート
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