反応式
[CH2:1]([NH2:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].N1[CH:14]=[CH:13]C=CC=1.C(OC(=O)C)(=[O:17])C>>[CH2:3]([CH2:2][C:1]([NH2:8])=[O:17])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:13][CH3:14]参加物
4
実験手順
Heptylamine (39 g; 0.34 mole was added dropwise to 46.6 g (0.59 mole) of pyridine and 43.4 g (0.43 mole) of acetic anhydride over 30 minutes, and the mixture was further stirred for 2 hours. After the reaction, the mixture was concentrated and extracted by adding water and ether. The ethereal layer was washed successively with a saturated aqueous solution of sodium hydrogen carbonate and then a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate and concentrated to give 51 g of the desired compound yield 96 %).
後処理
- customAfter the reaction
- concentrationthe mixture was concentrated
- extractionextracted
- additionby adding water and ether
- washThe ethereal layer was washed successively with a saturated aqueous solution of sodium hydrogen carbonate
- dry with materiala saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-92d48506e9a24c0e9213a9fa4487194a
- 出典データセット
- uspto-grants-1993_03
- 特許番号
- US05192799
関連ノート
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