戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 35762作成日:2026年10月24日

Sodium Hydroxide → 2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethyl-3-nitrophenyl)cyclohex-2-en-1-one

https://huagongshe.com/ja/reaction/35762

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物O-ethylhydroxylamine hydrochlorideHCID 76850—
反応物HCID 178458845HCID 178458845—
溶媒EthanolHCID 702—
生成物2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethyl-3-nitrophenyl)cyclohex-2-en-1-oneHCID 13620950183.2%

反応手順

Ethoxyamine hydrochloride (0.26 g; 2.7 mmole) and then sodium hydroxide (0.11 g; 2.7 mmole) were added to a solution of 3-hydroxy-5-(2,4,6-trimethyl-3-nitrophenyl)-2-propionylcyclohex-2-en-1-one (0.6 g; 1.8 mmole) in absolute ethanol (150 ml). The mixture was stirred at room temperature for a period of 18 hours and then the ethanol was removed by evaporation under reduced pressure. The residue was treated with dichloromethane and the organic phase was washed twice with water and dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure to give the product, 2-[1-(ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethyl-3-nitrophenyl)cyclohex-2-en-1one (0.56 g; 83.2%) as a pale yellow oil. The product was characterized by proton nuclear magnetic resonance spectroscopy and the spectroscopic data is recorded in Table 5, Example 37.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04767879
出典データセットuspto-grants-1988_08
ORD IDord-ea4ac235a9be4f3da8afc55c10b4281d
出典メモuspto-grants-1988_08