돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1381754생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1381754

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 washed twice with 200 ml ether each time. 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 번호US04803297
출처 데이터셋uspto-grants-1989_02
ORD IDord-f6002ed4566a40f4a3c4308f5756a2b0
출처 메모uspto-grants-1989_02