化工社化工社 化学情報印刷レポート · 研究参考用
Dimethylformamide → methyl (4E)-4-phenyl-4-[[4-[(5-phenyl-1,2-oxazol-3-yl)methoxy]phenyl]methoxyimino]butanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-(Chloromethyl)-5-phenyl-1,2-oxazole | HCID 1484769 | — |
| 反応物 | Ethyl acetate hexane | HCID 21226206 | — |
| 反応物 | 4-Hydroxybenzyloxyimino-4-phenylbutyrate | HCID 131722723 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | methyl (4E)-4-phenyl-4-[[4-[(5-phenyl-1,2-oxazol-3-yl)methoxy]phenyl]methoxyimino]butanoate | HCID 11730378 | 63% |
反応手順
A mixture of 3-(chloromethyl)-5-phenylisoxazole (340 mg), methyl E-4-(4-hydroxybenzyloxyimino-4-phenylbutyrate (500 mg), potassium carbonate (442 mg) and N,N-dimethylformamide (10 ml) was stirred at room temperature for 72 hours. Water was added to the reaction mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain methyl E-4-phenyl-4-[4-(5-phenyl-3-isoxazolylmethoxy)benzyloxyimino]butyrate (472 mg, yield 63%) as a colorless oil from an ethyl acetate-hexane (2:9, v/v)-eluted fraction.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06251926B1 |
| 出典データセット | uspto-grants-2001_06 |
| ORD ID | ord-32b3656aa86744a79e99edc5c2c75771 |
| 出典メモ | uspto-grants-2001_06 |