Ethanol → 2,5-nonanedione
反応式
[CH3:1][CH2:2][CH2:3][CH2:4][CH:5]=[O:6].[CH:7]([C:9]([CH3:11])=O)=[CH2:8].C(N(CC)CC)C.C([OH:21])C>>[CH3:1][C:2](=[O:21])[CH2:3][CH2:4][C:5](=[O:6])[CH2:8][CH2:7][CH2:9][CH3:11]参加物
5
実験手順
Following the procedure described in Example 1, 13.5 g (0.05 mol) of Cat. 1, 43.1 g (0.5 mol) of n-valeraldehyde, 35.1 g (0.5 mol) of methyl vinyl ketone, 500 ml of ethanol and 20.2 g (0.2 mol) of triethylamine are heated for 12 hours under nitrogen at the reflux temperature. For working up, the solvent is distilled, the cooled residue is taken up in chloroform, the chloroform phase is washed with dilute sulphuric acid and subsequently with water, the chloroform is removed and the liquid residue is distilled in a waterpump vacuum. Nonane-2,5-dione is obtained.
後処理
- distillationthe solvent is distilled
- washthe chloroform phase is washed with dilute sulphuric acid and subsequently with water
- customthe chloroform is removed
- distillationthe liquid residue is distilled in a waterpump vacuum
出典と根拠
- ORDレコード
- ord-03063fefccd84353b39346574fd8c449
- 出典データセット
- uspto-grants-1977_07
- 特許番号
- US04035395
反応ノート
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