反応式
C1(C)C=CC(S(O)(=O)=O)=CC=1.[CH3:12][CH:13]([SH:17])[CH:14]([SH:16])[CH3:15].[O:18]1[CH:22]=[CH:21][CH:20]=[C:19]1[CH:23]=O>C1CCCCC1>[O:18]1[CH:22]=[CH:21][CH:20]=[C:19]1[CH:23]1[S:17][CH:13]([CH3:12])[CH:14]([CH3:15])[S:16]1参加物
実験手順
Into a 100 ml reaction flask equipped with magnetic stirring bar, thermometer and reflux condenser and hot plate with magnetic stirring apparatus is placed 0.5 grams para-toluenesulfonic acid, 5 ml cyclohexane and 6.1 grams (0.05 moles) of 2,3-butanedithiol. Over a period of 35 minutes, 4.8 grams (0.05 moles) of 2-furaldehyde is added to the reaction mass with stirring. The reaction mass is then heated to reflux and refluxed for a period of 7.5 hours with stirring while removing water of reaction. After the refluxing period, the reaction mass is cooled to room temperature and transferred to a separatory funnel. The reaction mass is then washed with one 50 ml portion of saturated sodium chloride solution and dried over anhydrous sodium sulfate and filtered. The resulting filtrate is distilled using a Microvigreux column yielding the following fractions:
後処理
- customInto a 100 ml reaction flask
- customequipped with magnetic stirring bar
- temperaturethermometer and reflux condenser
- temperatureThe reaction mass is then heated
- temperatureto reflux
- temperaturerefluxed for a period of 7.5 hours
- stirringwith stirring
- customwhile removing
- customwater of reaction
- customtransferred to a separatory funnel
- washThe reaction mass is then washed with one 50 ml portion of saturated sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- distillationThe resulting filtrate is distilled
- customyielding the following fractions
出典と根拠
- ORDレコード
- ord-d4c2f66f3b2c455ab6ae07b7c9240dce
- 出典データセット
- uspto-grants-1985_05
- 特許番号
- US04515968
関連ノート
読み込み中…