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HRID 247238作成日:2026年10月24日

Triphenylphosphine → Ethanol, 2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]-

https://huagongshe.com/ja/reaction/247238

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Ammonium HydroxideHCID 14923—
反応物2-(2-(2-(2-Azidoethoxy)ethoxy)ethoxy)ethanolHCID 4614742—
溶媒PyridineHCID 1049—
生成物Ethanol, 2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]-HCID 160103—

反応手順

To a solution of Compound XXV (15.94 g; 72.7 mmole) in 100 ml of pyridine was added triphenylphosphine (29 g; 111 mmole). After stirring for one hour, at which time gas evolution had subsided, 50 ml of concentrated aqueous ammonium hydroxide was added and the mixture stirred overnight. The reaction mixture was concentrated under vacuum and the residue partitioned between 200 ml of water and 200 ml of ether (aqueous layer at pH 2). The aqueous layer was adjusted to pH 11 with solid sodium hydroxide and extracted three times with 150 ml n-butanol each time. The butanol extract was dried over sodium sulfate, filtered and concentrated. The residue was taken up in tetrahydrofuran and filtered. The filtrate was evaporated to a syrup which was azeotroped with toluene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04705886
出典データセットuspto-grants-1987_11
ORD IDord-3b5e34d6a8b74c77ad885ac681ae8b72
出典メモuspto-grants-1987_11