Hydrochloric Acid → 3,4-Dihydro-2,2-dimethyl-7-methoxy-3-(N-methyl-p-toluenesulfonamido)-1(2H)-naphthalenone
反応式
[CH3:1][C:2]([CH3:28])([CH:6]([N:16]([CH3:27])[S:17]([C:20]1[CH:25]=[CH:24][C:23]([CH3:26])=[CH:22][CH:21]=1)(=[O:19])=[O:18])[CH2:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[CH:10][CH:9]=1)[C:3](Cl)=[O:4].[Cl-].[Al+3].[Cl-].[Cl-].Cl>C1C=CC=CC=1>[CH3:1][C:2]1([CH3:28])[CH:6]([N:16]([CH3:27])[S:17]([C:20]2[CH:25]=[CH:24][C:23]([CH3:26])=[CH:22][CH:21]=2)(=[O:19])=[O:18])[CH2:7][C:8]2[C:13](=[CH:12][C:11]([O:14][CH3:15])=[CH:10][CH:9]=2)[C:3]1=[O:4]参加物
実験手順
To a cooled (with ice water) and stirred solution of 256 g of 2,2-dimethyl-4-(p-methoxyphenyl)-3-(N-methyl-p-toluenesulfonamido)butyryl chloride in 1500 ml of dry benzene 195 g of aluminium chloride is added rather rapidly. The mixture is stirred at room temperature for an additional 25 minutes and then poured on to a mixture of ice and 950 ml of concentrated hydrochloric acid. After stirring the mixture at room temperature for 30 minutes the organic layer is separated whereas the aqueous layer is shaken twice with benzene. The combined organic solutions are washed twice with water and again twice with an aqueous solution of potassium carbonate whereupon, after drying, the whole is concentrated in vacuo. The residue is taken up in ether which brings about the crystallization of the title product.
後処理
- additionis added rather rapidly
- stirringAfter stirring the mixture at room temperature for 30 minutes the organic layer
- customis separated whereas the aqueous layer
- stirringis shaken twice with benzene
- washThe combined organic solutions are washed twice with water and again twice with an aqueous solution of potassium carbonate whereupon,
- customafter drying
- concentrationthe whole is concentrated in vacuo
- custombrings about the crystallization of the title product
出典と根拠
- ORDレコード
- ord-aec8db8f30b741f49d5f520b875aa2bf
- 出典データセット
- uspto-grants-1978_12
- 特許番号
- US04128548
反応ノート
読み込み中…