Bromine → 1-Bromo-4,6,6-trichloro-3,3-dimethylhex-5-en-2-one
反応式
[Cl:1][C:2]([Cl:12])=[CH:3][CH:4]([Cl:11])[C:5]([CH3:10])([CH3:9])[C:6](=[O:8])[CH3:7].[Br:13]Br>C(Cl)(Cl)Cl>[Cl:1][C:2]([Cl:12])=[CH:3][CH:4]([Cl:11])[C:5]([CH3:9])([CH3:10])[C:6](=[O:8])[CH2:7][Br:13]参加物
4
実験手順
11.475 g (0.05 mol) of 1,1,3-trichloro-4,4-dimethyl-1-hexen-5-one are dissolved in 150 ml of chloroform, and 8 g (0.05 mol) of bromine are added without cooling. The mixture is stirred for 3 hours at room temperature, and hydrogen bromide and solvent are distilled off in vacuo; the final residues are removed in a high vacuum. 15.5 g are obtained of crude 1,1,3-trichloro-6-bromo-4,4-dimethyl-1-hexen-5-one, the structure of which is confirmed by the 1H-NMR spectrum. It is used directly in the next stage:
後処理
- temperaturewithout cooling
- distillationhydrogen bromide and solvent are distilled off in vacuo
- customthe final residues are removed in a high vacuum
出典と根拠
- ORDレコード
- ord-b6f9fe907bc041ffa649aa2aa9f3bc8e
- 出典データセット
- uspto-grants-1991_02
- 特許番号
- US04992577
反応ノート
読み込み中…