反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[CH2:9][CH2:10][CH2:11][N:12]1C(=O)C2C(=CC=CC=2)C1=O.C(O)C.NN>>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[CH2:9][CH2:10][CH2:11][NH2:12]参加物
4
実験手順
A 10 g (34.4 mmole) sample of the title compound of Example 33 was refluxed for 2 hours in 150 ml of ethanol containing 1.2 g (36.7 mmole) of 97% hydrazine. After concentrating the solution, the white crystalline residue was mixed with 100 ml of 10% NaOH and 100 ml of ether. The aqueous phase was separated and extracted with another 100 ml portion of ether. The combined ether extracts were than washed with water, dried over MgSO4 and stripped of all solvent under reduced pressure to yield 3.3 g (59%) of the product as an oil. This material was used without further purification.
後処理
- concentrationAfter concentrating the solution
- additionthe white crystalline residue was mixed with 100 ml of 10% NaOH and 100 ml of ether
- customThe aqueous phase was separated
- extractionextracted with another 100 ml portion of ether
- washthan washed with water
- dry with materialdried over MgSO4
出典と根拠
- ORDレコード
- ord-8c6d15244ef241f4a4b1f694d4b10335
- 出典データセット
- uspto-grants-1986_07
- 特許番号
- US04599325
関連ノート
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