Sulfuric Acid → 2-Phenyl-5-methoxy-6,7-dichloro-1-indanone
反応式
[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([C:9](=[O:18])[C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH2:11])[CH:5]=[CH:4][C:3]=1[O:19][CH3:20].S(=O)(=O)(O)O>C(Cl)Cl>[C:12]1([CH:10]2[CH2:11][C:5]3[C:6](=[C:7]([Cl:8])[C:2]([Cl:1])=[C:3]([O:19][CH3:20])[CH:4]=3)[C:9]2=[O:18])[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1参加物
実験手順
2,3-Dichloro-4-(2-phenylacryloyl)anisole (8.2 g., 26.8 mmol) in 215 ml. of methylene chloride is added dropwise over a 4.5 hr. period to a stirred solution of 107 ml. of sulfuric acid in 107 ml. of methylene chloride at 0°-5° under an atmosphere of argon. Following addition, the reaction mixture is stirred for 0.5 hr., poured over about 300 g. of crushed ice and the aqueous-organic phases separated. The aqueous phase is extracted with methylene chloride and the combine methylene chloride solutions sequentially washed with water and then dried over magnesium sulfate. Removal of the solvent affords 8.52 g. of solid which crystallized from benzene-cyclohexane provides 4.59 g. (56% yield) of 2-phenyl-5-methoxy-6,7-dichloro-1-indanone, m.p. 193.5°-196.5°.
後処理
- customat 0°-5°
- additionaddition
- addition, poured over about 300 g
- customof crushed ice and the aqueous-organic phases separated
- extractionThe aqueous phase is extracted with methylene chloride
- washthe combine methylene chloride solutions sequentially washed with water
- dry with materialdried over magnesium sulfate
- customRemoval of the solvent
- customaffords 8.52 g
- customof solid which crystallized from benzene-cyclohexane
- customprovides 4.59 g
出典と根拠
- ORDレコード
- ord-56d92672053a4e29b5159e72c1ce07d2
- 出典データセット
- uspto-grants-1982_06
- 特許番号
- US04334088
反応ノート
読み込み中…