反応式
[Na].[CH3:2][C:3]1[CH:8]=[CH:7][C:6]([SH:9])=[CH:5][CH:4]=1.Cl[CH:11](Cl)[C:12]([O:14][CH2:15][CH3:16])=[O:13]>CO.C(OCC)C>[CH3:2][C:3]1[CH:8]=[CH:7][C:6]([S:9][CH:11]([S:9][C:6]2[CH:7]=[CH:8][C:3]([CH3:2])=[CH:4][CH:5]=2)[C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:5][CH:4]=1参加物
反応条件
- 温度
- 20 °C
実験手順
Sodium (3.54 g) is dissolved in methanol (140 cc) and a solution of 4-methylthiophenol (21.8 g) in methanol (25 cc) is added. The mixture is stirred for 1 hour at 20° C. and a solution of ethyl dichloroacetate (12.5 g) in methanol (30 cc) is then added. The mixture is allowed to cool, the white precipitate obtained is filtered off, and the filtrate is concentrated to dryness under reduced pressure (20 mmHg) at 40° C. The oil obtained is taken up in diethyl ether (250 cc) and washed four times with N sodium hydroxide solution (50 cc each time) and four times with distilled water (50 cc each time). The ethereal phase is dried over anhydrous sodium sulphate, filtered, treated with animal charcoal, filtered and concentrated to dryness under reduced pressure (20 mmHg) at 40° C. Ethyl 2,2-bis(4-methylthiophenoxy)acetate (18 g) is thus obtained as a yellow oil.
後処理
- temperatureto cool
- customthe white precipitate obtained
- filtrationis filtered off
- concentrationthe filtrate is concentrated to dryness under reduced pressure (20 mmHg) at 40° C
- customThe oil obtained
- washwashed four times with N sodium hydroxide solution (50 cc each time) and four times with distilled water (50 cc each time)
- dry with materialThe ethereal phase is dried over anhydrous sodium sulphate
- filtrationfiltered
- additiontreated with animal charcoal
- filtrationfiltered
- concentrationconcentrated to dryness under reduced pressure (20 mmHg) at 40° C
出典と根拠
- ORDレコード
- ord-6bb31a9cb3cd4b5eaac488e1d6f003df
- 出典データセット
- uspto-grants-1980_09
- 特許番号
- US04225589
関連ノート
読み込み中…