化工社化工社 化学情報印刷レポート · 研究参考用
HRID 393365作成日:2026年10月24日
Water → 3-[4-chloro-2-fluoro-5-(2-nitrophenoxy)phenyl]-2-[(1-ethoxyethylidene)aminooxy]-6-trifluoromethyl-4(3H)-pyrimidinone
https://huagongshe.com/ja/reaction/393365
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Ethyl acetohydroximate | HCID 99894 | — |
| 反応物 | 2-chloro-3-[4-chloro-2-fluoro-5-(2-nitrophenoxy)phenyl]-6-trifluoromethyl-4(3H)-pyrimidinone | HCID 10238633 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-[4-chloro-2-fluoro-5-(2-nitrophenoxy)phenyl]-2-[(1-ethoxyethylidene)aminooxy]-6-trifluoromethyl-4(3H)-pyrimidinone | HCID 85335520 | 85% |
反応手順
Ethyl N-hydroxyacetimidate(0.23 g, 0.002 mol) was added dropwise to a suspension of sodium hydride(008 g, 0.002 mol) in tetrahydrofuran(5 ml) with stirring at 0° C. 2-Chloro-3-[4-chloro-2-fluoro-5-(2-nitrophenoxy)phenyl]-6-trifluoromethyl-4(3H)-pyrimidinone(0.93 g, 0.002 mol) was added to the mixture at 0° C., and the mixture was stirred at 0° C. for 3 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The ethyl acetate solution was concentrated and purified by column chromatography on silica gel(20% ethyl acetate/hexane) to give compound II-1 (0.90 g, yield 85%) as a white solid, m.p.152-155° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06806367B2 |
|---|
| 出典データセット | uspto-grants-2004_10 |
|---|
| ORD ID | ord-0462b6f913884dfabc6c95d62f226078 |
|---|
| 出典メモ | uspto-grants-2004_10 |
|---|