反応式
[O:1]=[C:2]([CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].Cl.[N:18](OCCCC)=[O:19]>C(O)C>[CH2:7]([O:6][C:4](=[O:5])[C:3](=[N:18][OH:19])[C:2](=[O:1])[CH2:9][CH2:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[CH3:8]参加物
5
実験手順
To a solution of 22.0 g. of ethyl 3-oxo-5-phenylvalerate in 100 ml. of ethanol is added 40 ml. of 38% hydrochloric acid, and after 10 minutes 11.3 ml. of n-butyl nitrite is added thereto. The resulting mixture is allowed to stand at room temperature for 45 minutes, and then the ethanol portion is essentially removed under reduced pressure to obtain an oily residue. The residue is poured into about 500 ml. of water and extracted 3 times with 200 ml. of chloroform. The combined extracts are dried over anhydrous sodium sulfate, then evaporated to obtain the title compound as a residue.
後処理
- customthe ethanol portion is essentially removed under reduced pressure
- customto obtain an oily residue
- additionThe residue is poured into about 500 ml
- extractionof water and extracted 3 times with 200 ml
- dry with materialThe combined extracts are dried over anhydrous sodium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-4fb8438852a245e4809299866b15c965
- 出典データセット
- uspto-grants-1977_08
- 特許番号
- US04042596
関連ノート
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