Methyl Ethyl Ketone → O-Naphthalen-2-yl (3-methoxyphenyl)methylcarbamothioate
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([N:9]([CH3:13])[C:10](Cl)=[S:11])[CH:6]=[CH:7][CH:8]=1.[CH:14]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=[CH:16][C:15]=1[OH:24].C(=O)([O-])[O-].[K+].[K+].C(C(C)=O)C>O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([N:9]([CH3:13])[C:10](=[S:11])[O:24][C:15]2[CH:16]=[CH:17][C:18]3[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:14]=2)[CH:6]=[CH:7][CH:8]=1参加物
実験手順
2.00 g of N-(3-methoxyphenyl)-N-methylthiocarbamoyl chloride, 1.44 g of β-naphthol and 1.66 g of anhydrous potassium carbonate were added to 50 ml of methyl ethyl ketone and heated to reflux for 15 hours. The reaction mixture was poured into water after it was cooled to room temperature and the products were extracted with benzene. The benzene solution was subsequently washed with water and aqueous saturated sodium chloride solution and then benzene was removed by distillation under reduced pressure after drying over anhydrous Magnesium sulfate. The residue was purified by the column chromatography (eluted with benzene on a silica gel) to give 1.45 g of O-2-naphthyl N-(3-methoxyphenyl)-N-methylthiocarbamate in crystalls (Yield: 45%). A part of the crystals was recrystallized from ethanol. Colorless crystalls having melting point of 93° to 94° C. were obtained.
後処理
- temperatureheated
- temperatureto reflux for 15 hours
- extractionthe products were extracted with benzene
- washThe benzene solution was subsequently washed with water and aqueous saturated sodium chloride solution
- custombenzene was removed by distillation under reduced pressure
- dry with materialafter drying over anhydrous Magnesium sulfate
- customThe residue was purified by the column chromatography (
- washeluted with benzene on a silica gel)
出典と根拠
- ORDレコード
- ord-d6949dcf117b49949f0c6fa219d26a5b
- 出典データセット
- uspto-grants-1985_11
- 特許番号
- US04551169
反応ノート
読み込み中…