反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1.[OH-:11].[Na+].C(Cl)(Cl)Cl>CC(C)=O>[C:8]([C:5]1[CH:6]=[CH:7][C:2]([O:1][C:5]([CH3:6])([CH3:4])[C:8]([OH:10])=[O:11])=[CH:3][CH:4]=1)(=[O:10])[CH3:9]参加物
5
実験手順
2-(p-Acetylphenoxy)-2-methylpropionic acid was prepared from 545 g. of p-hydroxyacetophenone, 960 g. of sodium hydroxide and 715 g. of chloroform in 11 liters of acetone according to the procedure described above in Example 1, part (d). The product was recrystallized from carbon tetrachloride and from isopropyl acetate to give 2-(p-acetylphenoxy)-2-methylpropionic acid as a pale cream solid, m.p. 108°-110°C.
後処理
- custom2-(p-Acetylphenoxy)-2-methylpropionic acid was prepared from 545 g
- customThe product was recrystallized from carbon tetrachloride and from isopropyl acetate
出典と根拠
- ORDレコード
- ord-43972321ca904c3ca0b13546863795ca
- 出典データセット
- uspto-grants-1976_04
- 特許番号
- US03948973
関連ノート
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