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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247238생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/247238

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Ammonium HydroxideHCID 14923—
반응물2-(2-(2-(2-Azidoethoxy)ethoxy)ethoxy)ethanolHCID 4614742—
용매PyridineHCID 1049—
생성물Ethanol, 2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]-HCID 160103—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04705886
출처 데이터셋uspto-grants-1987_11
ORD IDord-3b5e34d6a8b74c77ad885ac681ae8b72
출처 메모uspto-grants-1987_11