1,12-Dichlorododecane → Sodium Hydroxide
反応式
[CH2:1]([C:3]1[CH:9]=[CH:8][C:6]([O-:7])=[CH:5][CH:4]=1)[CH3:2].[Na+:10].Cl[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]Cl>>[CH2:1]([C:3]1[CH:9]=[CH:8][C:6]([O:7][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][O:7][C:6]2[CH:8]=[CH:9][C:3]([CH2:1][CH3:2])=[CH:4][CH:5]=2)=[CH:5][CH:4]=1)[CH3:2].[OH-:7].[Na+:10]参加物
4
実験手順
1,12-bis (4-ethylphenoxy) dodecane is prepared from sodium 4-ethylphenoxide and 1,12-dichlorododecane, according to the method of Example 1, and sulfonated to the disulfonic acid derivative and neutralized with sodium hydroxide according to the method of Example 2, to afford the disodium sulfonate derivative.
出典と根拠
- ORDレコード
- ord-08439230fa134c5e9c08f0a63023873c
- 出典データセット
- uspto-grants-1981_12
- 特許番号
- US04307078
反応ノート
読み込み中…