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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 984750생성일: 2026년 10월 25일

Carbon Dioxide → 8-Oxatricyclo(7.4.0.0,2,7)trideca-1(9),2(7),3,5,10,12-hexaene-6-carboxylic acid

https://huagongshe.com/reaction/984750

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물DibenzofuranHCID 568—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매Sodium HydroxideHCID 14798—
생성물8-Oxatricyclo(7.4.0.0,2,7)trideca-1(9),2(7),3,5,10,12-hexaene-6-carboxylic acidHCID 30287258%

반응 조건

온도20 °C

반응 단계

A solution of 1.6M n-butyllithium in hexane (18.5 ml) was added dropwise to a stirred solution of dibenzofuran (5.0 g) in anhydrous THF (25 ml) at −78° C. under a nitrogen atmosphere. The resulting suspension was allowed to warm to 20° C. where it was stirred for 3 h. It was then cooled to −78° C. and added to a mixture of excess solid carbon dioxide in diethyl ether (250 ml) under a nitrogen atmosphere. The resulting white suspension was allowed to stand for 1 h at 20° C. and was then diluted with 2M sodium hydroxide (500 ml). The aqueous extract was washed with ether (3×200 ml), acidified to pH 1 with 6M hydrochloric acid and extracted with ethyl acetate (3×200 ml). The combined organic extracts were washed with brine (50 ml), dried over magnesium sulphate and evaporated in vacuo to give the title compound as a white solid (3.64 g, 58%). LCMS: Rt 5.06 min; m/z 213 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06867192B1
출처 데이터셋uspto-grants-2005_03
ORD IDord-3b2ff2473bb642a7969c2a0d8e22661c
출처 메모uspto-grants-2005_03