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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395888생성일: 2026년 10월 26일

8-Oxabicyclo[3.2.1]oct-6-en-3-one → HCID 178456493, 화합물

https://huagongshe.com/reaction/395888

반응식

참여 물질

역할이름HCID투입량
반응물8-Oxabicyclo[3.2.1]oct-6-en-3-oneHCID 557672—
반응물8-(8-Hydroxy-8-methyl-bicyclo[3.2.1]oct-3-yl)-1,3-dipropyl-3,7-dihydro-purine-2,6-dioneHCID 18173101—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물HCID 178456493HCID 178456493—

반응 단계

To a stirred solution of 1,3-dipropyl-7-pyrrolidin-1-ylmethyl-3,7-dihydro-purine-2,6-dione (Example 48) (522 mg, 1.63 mmol) in THF (50 ml) at −78° C. was added n-BuLi (1.55 M in hexanes, 1.2 eq, 1.3 ml). The color of the resulting yellow mixture deepened to orange-red and was stirred at this temperature for 0.5 h. A solution of 8-oxa-bicyclo[3.2.1]oct-6-en-3-one (1.1 eq, 222 mg, 1.79 mmol) in THF (4 ml) was added via syringe over a period of 20 minutes. The mixture was held at −78° C. for 2 h and allowed to reach ambient temperature overnight (12 h). The reaction mixture was partitioned between saturated aqeuous NH4Cl (20 ml) and EtOAc (20 ml) and the aqueous phase was extracted with EtOAc (20 ml). The combined organic extracts were washed with saturated aqeuous NaCl (20 ml), dried (MgSO4), filtered and concentrated in vacuo. The resulting orange oil was purified by chromatography on silica using 5% MeOH in CH2Cl2 as eluent to give a clear oil that solidified upon standing (50 mg, 8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605600B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-2f7ed1c428dc4bc2831aeccb59e669aa
출처 메모uspto-grants-2003_08