Anthranilic Acid → 1,3-Dithiaindane, 2-(3-methylbutyl)oxy-
反応式
[CH2:1]([OH:6])[CH2:2][CH:3]([CH3:5])[CH3:4].[C:7](=[S:9])=[S:8].C(O)(=O)[C:11]1[C:12](=[CH:14][CH:15]=[CH:16][CH:17]=1)N>ClCCCl.O1CCOCC1>[CH2:1]([O:6][CH:7]1[S:9][C:17]2[CH:16]=[CH:15][CH:14]=[CH:12][C:11]=2[S:8]1)[CH2:2][CH:3]([CH3:5])[CH3:4]参加物
反応条件
- 温度
- 80 °C
実験手順
42.1 g (0.36 mole) of isoamyl nitrile, 52.8 g (0.60 mole) of isoamyl alcohol and 150 ml of carbon disulfide were dissolved in 800 ml of 1,2-dichloroethane. The reaction solution was mildly heated under reflux at a temperature of about 80° C. A solution of 41.1 g (0.30 mole) of anthranilic acid in 100 ml of dioxane was added dropwise to the reaction solution over 1.5 hours. The reaction solution was further heated under reflux for an additional 30 minutes. The resulting mixture was washed successively with water, a saturated aqueous solution of sodium carbonate and water, and then dried over magnesium sulfate. The resulting organic solution was concentrated under reduced pressure. The residue was then purified through silica gel column chromatography (75 to 230 mesh; eluent: benzene) to obtain 28.8 g (yield: 40%) of the desired compound (V) as a pale yellow oil. The physical properties of the compound were as follows:
後処理
- temperatureThe reaction solution was mildly heated
- temperatureThe reaction solution was further heated
- temperatureunder reflux for an additional 30 minutes
- washThe resulting mixture was washed successively with water
- dry with materiala saturated aqueous solution of sodium carbonate and water, and then dried over magnesium sulfate
- concentrationThe resulting organic solution was concentrated under reduced pressure
- customThe residue was then purified through silica gel column chromatography (75 to 230 mesh; eluent: benzene)
出典と根拠
- ORDレコード
- ord-b04ebeed25cb4373ae090a505820565d
- 出典データセット
- uspto-grants-1993_07
- 特許番号
- US05229238
反応ノート
読み込み中…