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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2285556생성일: 2026년 10월 26일

2-((Acetyloxy)methoxy)ethyl acetate → 2-((2,6-Dichloro-9H-purin-9-yl)methoxy)ethyl acetate

https://huagongshe.com/reaction/2285556

반응식

참여 물질

역할이름HCID투입량
반응물2-((Acetyloxy)methoxy)ethyl acetateHCID 100999—
반응물2,6-DichloropurineHCID 5324412—
용매Diethyl EtherHCID 3283—
생성물2-((2,6-Dichloro-9H-purin-9-yl)methoxy)ethyl acetateHCID 38766664%

반응 조건

온도138 °C

반응 단계

2,6-Dichloropurine 5.5 g and 2-oxa-1,4-butanediol diacetate 513 g were placed in a flask and partially evacuated and then heated to 138° C., initially the mixture was too thick to stir but gradually gave rise to a melt which was stirred, and after 20 minutes was completely melted and the reaction mixture heated for 10 minutes more (total heat time=30 minutes). The mixture was then cooled to room temperature and para-toluenesulphonic acid 150 mg was added, the vacuum reapplied and heating resumed with stirring. After 20 minutes heating vigorous bubbling was noted; the mixture was cooled to room temperature; chloroform was added, and the solution was extracted once with saturated aqueous sodium bicarbonate and once with water. The chloroform phase was dried over anhydrous sodium sulphate and evaporated. The residual oil was dissolved in benzene and applied to a column of 200 g. of silica gel in benzene. Benzene elution removed the acetate by-products. Ether solution gave 2,6-dichloro-9-(2-acetyloxyethoxymethyl)purine (64% yield). Recrystallization from benzene gave lustrous white flakes, m.p. 96°-99° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04323573
출처 데이터셋uspto-grants-1982_04
ORD IDord-5c5fadd32d4e4dd6b62225840002223f
출처 메모uspto-grants-1982_04