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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1375138생성일: 2026년 10월 25일

Carbon Dioxide → 3-hydroxy-4-methoxynaphtho[2,3-c]furan-1(3H)-one

https://huagongshe.com/reaction/1375138

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Hydrochloric AcidHCID 313—
반응물1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
반응물1-Methoxynaphthalene-2-carbaldehydeHCID 13119993—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-hydroxy-4-methoxynaphtho[2,3-c]furan-1(3H)-oneHCID 210793353.7%

반응 조건

온도-20 °C

반응 단계

N,N,N′-Trimethylethylene diamine (0.82 ml, 6.3 mmol) was dissolved in tetrahydrofuran (16 ml) and cooled to −20° C. n-Butyl lithium (1.6M in hexanes, 3.9 ml, 6.24 mmol) was added and the reaction stirred at −20° C. for 15 min. 1-Methoxy-2-naphthaldehyde (0.96 g, 5.9 mmol) was added followed by n-butyl lithium (1.6M in hexanes, 11.25 ml, 18 mmol) and the reaction stirred at 25° C. for 3 h. Solid carbon dioxide was added and the reaction left until the excess carbon dioxide had sublimed. Stirring continued for 15 min before addition of hydrochloric acid (2N, 50 ml). The mixture was extracted with dichloromethane (50 ml, ×3). The combined extracts were dried (MgSO4) and the solvent evaporated under vacuum. The oily residue was preabsorbed onto silica and purified by SPE (silica, 10 g) eluting with an ethyl acetate/cyclohexane gradient to give 3-hydroxy-4-methoxynaphtho[2,3-c]furan-1 (3H)-one (50 mg, 3.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07166631B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-d03b82f4bcb0400b96f95b1ba5da9854
출처 메모uspto-grants-2007_01