反応式
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1)[CH3:2].[Br:10]Br>C(Cl)(Cl)Cl>[Br:10][C:5]1[CH:4]=[C:3]([CH2:1][CH3:2])[CH:8]=[CH:7][C:6]=1[OH:9]参加物
4
実験手順
A solution was prepared by dissolving 105 g of 4-ethylphenol into 500 ml of chloroform. The solution was cooled by ice water bath, followed by dropwise addition of 45 ml of bromine while stirring. The addition was took 1 hour. Then, the reaction mixture was cooled by an ice water bath while stirring for 4 hours, moved into a separatory funnel to wash with water, an aqueous solution saturated with NaCl, 10% water solution of sodium hydrogencarbonate and an aqueous solution saturated with NaCl in turn, and dried with magnesium sulfate anhydride. The solvent in the reactant was distilled off under reduced pressure to yield 173 g of light brown and oily 2-bromo-4-ethylphenol.
後処理
- customA solution was prepared
- temperatureThe solution was cooled by ice water bath
- additionThe addition
- temperatureThen, the reaction mixture was cooled by an ice water bath
- stirringwhile stirring for 4 hours
- custommoved into a separatory funnel
- washto wash with water
- dry with materialan aqueous solution saturated with NaCl, 10% water solution of sodium hydrogencarbonate and an aqueous solution saturated with NaCl in turn, and dried with magnesium sulfate anhydride
- distillationThe solvent in the reactant was distilled off under reduced pressure
出典と根拠
- ORDレコード
- ord-c6946c29b9434897a7e6e019ab9f0653
- 出典データセット
- uspto-grants-1991_10
- 特許番号
- US05053548
関連ノート
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