HCl butanone → HCID 67152368、化合物

HRID 1677853ノート

反応式

HRID 1677853 の反応式
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

3

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

  1. temperaturewas refluxed for 2 hours
  2. customThe butanone was evaporated in vacuo
  3. extractionThe aqueous solution was extracted with diethyl ether (2×50 mL)
  4. customthe aqueous layer was collected
  5. extractionextracted with dichloromethane (2×50 mL)
  6. dry with materialThe combined dichloromethane extracts were dried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customto yield the crude title compound
  9. customThe product was crystallized
  10. customby triturating in diethyl ether
  11. 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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