Sulfuric Acid → HCID 13924084, compound

Participants

Reaction Conditions

Reaction Steps

All work is performed an inert atmosphere using anhydrous tetrahydrofuran. The starting material, 3-(5-cyclopenten-3-yl) valeraldehyde {2-cyclopentene-1-pentanal} (75 g, 0.493 moles) is diluted in tetrahydrofurar (750 ml) and cooled in a -30° C. ethanol/dry ice bath. Ethyl magnesium bromide (0.493 moles) is added dropwise to the stirring reaction mixture for a period of over 2 hours. The mixture is warmed to 0° C. and water (100 ml), followed by 15% sulfuric acid (200 ml), is added and the organic phase separated. The aqueous layer is extracted with ether (2×300 ml) and the organic extracts are combined. The volume is reduced and the residue washed with brine (400 ml). The product is dried over anhydrous sodium sulfate and the remaining solvent removed under vacuum leaving a clear yellow oil. The crude product is chromatographed on silica gel and subsequently kugelrohred under vacuum leaving clear, colorless oil (10.2 g, 0.056 moles).

Provenance & Evidence