Water → HCID 57545186、化合物
反応式
C[O:2][C:3](=[O:25])[CH:4]([C:18]1[CH:23]=[CH:22][C:21]([Br:24])=[CH:20][CH:19]=1)[O:5][C:6]1[CH:11]=[C:10]([O:12][CH2:13][CH3:14])[CH:9]=[C:8]([O:15][CH2:16][CH3:17])[CH:7]=1.O.C(=O)([O-])[O-].[K+].[K+]>CO>[Br:24][C:21]1[CH:20]=[CH:19][C:18]([CH:4]([O:5][C:6]2[CH:7]=[C:8]([O:15][CH2:16][CH3:17])[CH:9]=[C:10]([O:12][CH2:13][CH3:14])[CH:11]=2)[C:3]([OH:25])=[O:2])=[CH:23][CH:22]=1参加物
5
実験手順
16.9 g (41.3 mmol) of methyl(4-bromophenyl)-(3,5-diethoxyphenoxy)acetate are dissolved in 80 ml of methanol and 8 ml of water under argon at RT, and 7.99 g (57.8 mmol) of potassium carbonate are added. The mixture is heated under RF for 4 h. After cooling, the precipitate is filtered off, the filtrate is concentrated, the residue is taken up in water and the solution is extracted four times with diethyl ether. The aqueous phase is adjusted to a pH of 2 by adding 10% strength hydrochloric acid and is extracted three times with ethyl acetate, and the combined ethyl acetate phases are washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated. 16.1 g (99% of theory) of the product are obtained.
後処理
- temperatureThe mixture is heated under RF for 4 h
- temperatureAfter cooling
- filtrationthe precipitate is filtered off
- concentrationthe filtrate is concentrated
- extractionthe solution is extracted four times with diethyl ether
- additionby adding 10% strength hydrochloric acid
- extractionis extracted three times with ethyl acetate
- washthe combined ethyl acetate phases are washed with saturated sodium chloride solution
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- custom16.1 g (99% of theory) of the product are obtained
出典と根拠
- ORDレコード
- ord-19482c96379b47138c2ad592573849b3
- 出典データセット
- uspto-grants-2011_10
- 特許番号
- US08030347B2
反応ノート
読み込み中…