Hydrochloric Acid → 1-Benzyl-3-(1,3-dithiol-2-ylidene)-5-methyl-2,4-dioxopiperidine
反応式
[CH2:1]([N:8]1[C:13](=[O:14])[C:12](=[C:15]2[S:19][CH:18]=[CH:17][S:16]2)[C:11](=[O:20])[C:10](C)([C:21](OCC)=O)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].Cl.O>C(O)C>[CH2:1]([N:8]1[CH2:9][CH:10]([CH3:21])[C:11](=[O:20])[C:12](=[C:15]2[S:19][CH:18]=[CH:17][S:16]2)[C:13]1=[O:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
実験手順
Ethyl 1-benzyl-5-(1,3-dithiol-2-ylidene)-3-methyl-4,6-dioxopiperidine-3-carboxylate (245 mg) is dissolved in ethanol (5 ml), and thereto is added a 10% sodium hydroxide solution (2.5 ml). The mixture is stirred at room temperature overnight. The mixture is acidified with 10% HCl, and poured into water. The aqueous solution is extracted with ethyl acetate. The extract is washed with a saturated sodium chloride solution, dried and then distilled to remove the solvent. The residue is dissolved in ethanol (20 ml) and the solution is refluxed for one hour. The mixture is distilled to remove the solvent. The residue is purified by silica gel column chromatography (solvent, ethyl acetate:n-hexane=1:1), and is recrystallized from a mixture of ethyl acetate and n-hexane to give 1-benzyl-3-(1,3-dithiol-2-ylidene)-5-methyl-2,4-dioxopiperidine (138 mg, 69.1%) as pale yellow needles, m.p. 168°-170° C.
後処理
- extractionThe aqueous solution is extracted with ethyl acetate
- washThe extract is washed with a saturated sodium chloride solution
- customdried
- distillationdistilled
- customto remove the solvent
- dissolutionThe residue is dissolved in ethanol (20 ml)
- temperaturethe solution is refluxed for one hour
- distillationThe mixture is distilled
- customto remove the solvent
- customThe residue is purified by silica gel column chromatography (solvent, ethyl acetate:n-hexane=1:1)
- customis recrystallized from a mixture of ethyl acetate and n-hexane
出典と根拠
- ORDレコード
- ord-628112997dbd4cf6af8955a1426eba4e
- 出典データセット
- uspto-grants-1987_05
- 特許番号
- US04663319
反応ノート
読み込み中…