反応式
[C:1]1([C@@H:7]2[CH2:11][CH2:10][CH2:9][C@H:8]2[NH:12][S:13]([CH:16]([CH3:18])[CH3:17])(=[O:15])=[O:14])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)O.II.O=[I:27](OI(=O)=O)=O.S(=O)(O)[O-].[Na+]>C(O)(=O)C>[I:27][C:4]1[CH:3]=[CH:2][C:1]([C@@H:7]2[CH2:11][CH2:10][CH2:9][C@H:8]2[NH:12][S:13]([CH:16]([CH3:18])[CH3:17])(=[O:15])=[O:14])=[CH:6][CH:5]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 90 °C
実験手順
(+,−) Trans-propane-2-sulfonic acid (2-phenyl-cyclopentyl)-amide (0.52 g, 1.47 mmol, prepared in example 1) was dissolved in 30 mL of glacial acetic acid. To this solution was added concentrated sulfuric acid (0.16 mL, 1.61 mmol) at room temperature followed by iodine (0.19 g, 0.74 mmol), and diiodine pentoxide (0.20 g, 0.59 mmol). The reaction was then protected from light and heated to 90° C. and stirred for 22 hours. To the dark brown reaction mixture was slowly added 10% aqueous sodium bisulfite. The mixture was cooled to 0° C. for 1 hour and a light brown solid collected by filtration. The solid was dissolved in warm diethyl ether and washed with water (2×), then saturated sodium bicarbonate (1×). The organic layer was separated, dried (Na2SO4), filtered and concentrated in vacuo to give 435 mg (75%) of the title compound. The NMR was consistent with the assigned structure.
後処理
- temperatureThe mixture was cooled to 0° C. for 1 hour
- filtrationa light brown solid collected by filtration
- dissolutionThe solid was dissolved in warm diethyl ether
- washwashed with water (2×)
- customThe organic layer was separated
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-1340a906f63c415a8cfb501561f1444f
- 出典データセット
- uspto-grants-2003_10
- 特許番号
- US06639107B1
関連ノート
読み込み中…