戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 584385作成日:2026年10月26日

Hydrochloric Acid → methyl (4E)-4-[(4-hydroxyphenyl)methoxyimino]-4-phenylbutanoate

https://huagongshe.com/reaction/584385

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzenebutanoic acid, gamma-oxo-, methyl esterHCID 141190—
反応物Sodium AcetateHCID 517045—
反応物4-MethoxymethoxybenzyloxyamineHCID 11052292—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物methyl (4E)-4-[(4-hydroxyphenyl)methoxyimino]-4-phenylbutanoateHCID 1094692950%

反応手順

A mixture of 4-methoxymethoxybenzyloxyamine (4.99 g), methyl 4-oxo-4-phenylbutyrate (5.71 g), acetic acid (5.10 ml), sodium acetate (4.87 g) and methanol (200 ml) was heated under reflux for 15 hours. The reaction mixture was cooled to room temperature, dilute hydrochloric acid was added to the residue 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 dissolved in tetrahydrofuran (50 ml) and methanol (5 ml). To this solution was added 1N hydrochloric acid (10 ml) and heated under reflux for 3 hours. The reaction mixture was cooled to room temperature, water was added 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-(4-hydroxybenzyloxyimino)-4-phenylbutyrate (4.24 g, yield 50%) as a colorless oil from an ethyl acetate-hexane (2:5, v/v)-eluted fraction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06924300B2
出典データセットuspto-grants-2005_08
ORD IDord-2b41ece8d71e4fb6b3c7eadcd86174d1
出典メモuspto-grants-2005_08