Tetrahydrofuran → HCID 19759295、化合物
反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]3[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=3[CH:9]=2)=[CH:4][CH:3]=1.[O:17]1CCC[CH2:18]1.C([Li])CCC>CN(C)C=O>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]3[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=3[C:9]=2[CH:18]=[O:17])=[CH:4][CH:3]=1参加物
反応条件
- 温度
- -78 °C
実験手順
To a solution of 2-(4-methylphenyl)benzo[b]thiophene (896 mg) in freshly distillated tetrahydrofuran (15 ml) was added n-butyllithium (2.75 ml, 1.6 mol solution in n-hexane) through a syringe at -78° C. The solution was stirred at -78° C. for 10 minutes and then at ambient temperature for half an hour. To the deep red colored solution was added N,N-dimethylformamide (365mg) at 5° C. The mixture was stirred at ambient temperature for one hour, quenched with aqueous saturated ammonium chloride solution, and extracted with diethyl ether. The organic layer was washed with aqueous saturated ammonium chloride solution, dried, and concentrated in vacuo to give a yellow residue, which was purified by flash column chromatography on silica gel eluted with 50% n-hexane in dichloromethane to yield 2-(4-methylphenyl)benzo[b]thiophene-3-carbaldehyde (285 mg) as white crystals.
後処理
- waitat ambient temperature for half an hour
- stirringThe mixture was stirred at ambient temperature for one hour
- customquenched with aqueous saturated ammonium chloride solution
- extractionextracted with diethyl ether
- washThe organic layer was washed with aqueous saturated ammonium chloride solution
- customdried
- concentrationconcentrated in vacuo
- customto give a yellow residue, which
- customwas purified by flash column chromatography on silica gel
- washeluted with 50% n-hexane in dichloromethane
出典と根拠
- ORDレコード
- ord-19ab70f4917b4ca7a518ef753b060680
- 出典データセット
- uspto-grants-1993_06
- 特許番号
- US05215994
反応ノート
読み込み中…