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

Temperatur

-20 °C

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%).

1. additionwas added
2. stirringthe reaction stirred at 25° C. for 3 h
3. stirringStirring
4. extractionThe mixture was extracted with dichloromethane (50 ml, ×3)
5. dry with materialThe combined extracts were dried (MgSO4)
6. customthe solvent evaporated under vacuum
7. customThe oily residue was preabsorbed onto silica
8. custompurified by SPE (silica, 10 g)
9. washeluting with an ethyl acetate/cyclohexane gradient

ORD-Eintrag

ord-d03b82f4bcb0400b96f95b1ba5da9854

Quelldatensatz

uspto-grants-2007_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07166631B2