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HRID 1052898作成日:2026年10月27日

Water → 3-[3-Benzyloxy-3-(4-fluoro-phenyl)-propyl]-4-(4-benzyloxy-phenyl)-1-(4-fluoro-phenyl)-azetidin-2-one

https://huagongshe.com/reaction/1052898

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TolueneHCID 1140—
反応物trimethylsilyl N-trimethylsilylethanimidateHCID 25248—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物5-Benzyloxy-2-[(4-benzyloxy-phenyl)-(4-fluoro-phenylamino)-methyl]-5-(4-fluoro-phenyl)-pentanoic acid methyl esterHCID 66713420—
生成物3-[3-Benzyloxy-3-(4-fluoro-phenyl)-propyl]-4-(4-benzyloxy-phenyl)-1-(4-fluoro-phenyl)-azetidin-2-oneHCID 66713280—

反応手順

2 gms of 5-Benzyloxy-2-[(4-benzyloxy-phenyl)-(4-fluoro-phenylamino)-methyl]-5-(4-fluoro-phenyl)-pentanoic acid methyl ester was dissolved in 20 ml of toluene and stirred at room temperature for 5-20 minutes. To the reaction mass 2.39 ml of N,O-Bis-(trimethylsilyl)-acetamide was added and temperature was raised to 40-60° C. To this 0.04 gms of Tetra butyl ammonium fluoride was added and reaction was monitored by TLC. Water was added and organic fraction was distilled to get 1.5 gms of 3-[3-Benzyloxy-3-(4-fluoro-phenyl)-propyl]-4-(4-benzyloxy-phenyl)-1-(4-fluoro-phenyl)-azetidin-2-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09388440B2
出典データセットuspto-grants-2016_07
ORD IDord-17fd14a86c0e44c4959782ed675e4770
出典メモuspto-grants-2016_07