돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1378712생성일: 2026년 10월 25일

Methanol → 2-Fluoroadenosine

https://huagongshe.com/reaction/1378712

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물ChloroformHCID 6212—
반응물Sodium HydroxideHCID 14798—
반응물2',3',5'-Tri-O-acetyl-2-fluoroadenosineHCID 21816271—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물2-FluoroadenosineHCID 8975—

반응 단계

2-Fluoro-2',3',5'-tri-O-acetyladenosine (0.41 g, 10 mmol) was dissolved in a mixture of 1,4-dioxane (7 mL) and water (2 mL) and the solution was cooled in an icewater bath. 2.5M NaOH (1.40 mL, 3.5 mmol) was added dropwise with vigorous stirring over a 2 min. period. The resulting bright yellow solution was stirred at 0° C. and monitored by TLC (9:1 Chloroform:methanol). After 2 hours, most of the yellow color had faded and TLC showed no acetylated intermediates remaining. The homogeneous reaction mixture was poured directly onto a column of AG 50-X4 (H+, 100-200 mesh, 10 mL bed volume) ion exchange resin and the column was eluted with several column volumes of 1:1 methanol:water. 2-Fluoroadenosine began to elute immediately, and all fractions which contained 2-fluoroadenosine were concentrated under vacuum to obtain a white partially crystalline solid which was dried overnight at 60° C. under vacuum: 0.20 g (70% yield), mp 220°-227° C. (d). This material was consistent by TLC, IR and UV with an authentic sample of 2-fluoroadenosine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05668270
출처 데이터셋uspto-grants-1997_09
ORD IDord-a98569d7c6024972885b818bf8e81d12
출처 메모uspto-grants-1997_09