反応式
[C:1]([O:6][OH:7])([CH2:4][CH3:5])([CH3:3])[CH3:2].OC([C:12]1[CH:17]=[CH:16][C:15]([C:18]([OH:21])([CH3:20])[CH3:19])=[CH:14][CH:13]=1)(C)C.S(=O)(=O)(O)O>O>[C:1]([O:6][O:7][C:12]([C:13]1[CH:12]=[CH:17][CH:16]=[C:15]([C:18]([O:21][O:21][C:18]([CH2:15][CH3:14])([CH3:20])[CH3:19])([CH3:19])[CH3:20])[CH:14]=1)([CH3:17])[CH3:13])([CH2:4][CH3:5])([CH3:3])[CH3:2]参加物
5
実験手順
1,4-Bis(2-t-amylperoxy-2-propyl)benzene (para III) was prepared by reacting 28.1 grams (0.231 mole) of aqueous 85.7% t-amyl hydroperoxide diluted with 3.2 grams of water with 20.4 grams (0.105 mole) of 1,4-bis(2-hydroxy-2-propyl)benzene in the presence of 44.1 grams (0.316 mole) of 70% sulfuric acid according to the procedure of Example VII. The stripped product was a yellow liquid which remained liquid at 15° C. The product weighed 32.0 grams.
後処理
- customat 15° C
出典と根拠
- ORDレコード
- ord-4a4d45c4eb9243e2a9facd98ed10c5f3
- 出典データセット
- uspto-grants-1996_07
- 特許番号
- US05539061
関連ノート
読み込み中…