反応式
[CH3:1][O:2][CH2:3][CH2:4]O.[CH3:6][O:7][C:8](=[O:18])[C:9]1[CH:14]=[C:13]([Cl:15])[C:12]([OH:16])=[C:11]([Cl:17])[CH:10]=1.[OH-:19].[Na+].Br[CH2:22][C:23]1[C:28]([Br:29])=[C:27]([Br:30])[C:26]([Br:31])=[C:25]([CH2:32]Br)[C:24]=1[Br:34].[OH2:35]>>[C:8]([C:9]1[CH:10]=[C:11]([Cl:17])[C:12]([O:16][CH2:22][C:23]2[C:28]([Br:29])=[C:27]([Br:30])[C:26]([Br:31])=[C:25]([CH2:32][O:19][C:12]3[C:13]([Cl:15])=[CH:14][C:4]([C:3]([O:2][CH3:1])=[O:35])=[CH:10][C:11]=3[Cl:17])[C:24]=2[Br:34])=[C:13]([Cl:15])[CH:14]=1)([O:7][CH3:6])=[O:18]参加物
6
実験手順
In a four-liter reaction vessel, 3 liters of methyl glycol (B.P. 122°-126° C.), 221 g (1 mole) of 3,5-dichloro-4-hydroxybenzoic acid methyl ester, 40 g (1 mole) of sodium hydroxide in 40 ml of water, and 289.8 g (0.5 mole) of 1,3-bis-(bromomethyl)-2,4,5,6-tetrabromobenzene were reacted and worked up in the manner described in Example 46.
後処理
- customwere reacted
出典と根拠
- ORDレコード
- ord-e26386e68cc4414b80148d386f0c134c
- 出典データセット
- uspto-grants-1979_05
- 特許番号
- US04152511
関連ノート
読み込み中…