Sulfuric Acid → 3-(2,4-Dichlorobenzoyl)pentane-2,4-dione
反応式
[O-:1][CH2:2][CH3:3].[Mg+2].[O-:5][CH2:6][CH3:7].[Cl:8][C:9]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:10]=1[C:11](Cl)=[O:12].S(=O)(=O)(O)O.[CH3:24]COCC>>[Cl:8][C:9]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:10]=1[C:11]([CH:3]([C:6](=[O:5])[CH3:7])[C:2](=[O:1])[CH3:24])=[O:12]参加物
実験手順
A mixture of magnesium ethoxide (22.9 g, 0.2 moles) 2,4-pentanedione (20.0 g, 0.2 moles), and ether (150 ml) was heated at reflux for 1 hour. 2,4-Dichlorobenzoyl chloride (41.9 g, 0.2 mole) in ether (50 ml) was added to the mixture over a period of 15 minutes, and the resultant mixture was heated at reflux for an additional 0.5 hour. After cooling, the reaction mixture was poured into 200 ml of 10% sulfuric acid. The ether layer was separated and stirred with 250 ml of 5% copper (II) acetate. The resulting copper salt was filtered, washed with ether, and stirred with 6N hydrochloric acid to destroy the salt. The acidic aqueous solution was extracted with ether. The ether extract was washed with saturated sodium chloride, dried over anhydrous magnesium sulfate, and concentrated under vacuum yielding 21 g of the desired product as a yellow oil. It was identified as such by nuclear magnetic resonance spectroscopy, infrared spectroscopy, and mass spectroscopy.
後処理
- temperaturewas heated
- temperatureat reflux for 1 hour
- temperatureat reflux for an additional 0.5 hour
- temperatureAfter cooling
- customThe ether layer was separated
- filtrationThe resulting copper salt was filtered
- washwashed with ether
- stirringstirred with 6N hydrochloric acid
- customto destroy the salt
- extractionThe acidic aqueous solution was extracted with ether
- extractionThe ether extract
- washwas washed with saturated sodium chloride
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under vacuum
出典と根拠
- ORDレコード
- ord-2479c9b791c1431f9fc527ffd40080cb
- 出典データセット
- uspto-grants-1988_05
- 特許番号
- US04741769
反応ノート
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