2-Furancarboxylic acid, 5-methyl- → 5-Methyloxolane-2-carboxylic acid

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Reaction Steps

A solution of 5-methyl-2-furoic acid (3.65 g, 28.97 mmol) in ethyl acetate (60 ml) was hydrogenated over 5% rhodium on carbon (250 mg) until hydrogen uptake ceased. The catalyst was filtered off and washed with ethyl acetate. The combined filtrates were concentrated in vacuo to yield the title compound as a pale yellow oil (3.67 g, 97%); νmax (CH2Cl2) 3384, 3359, 1775, 1724 and 1355 cm-1 ; δH (CDCl3, 250 MHz) 1.35 (3 H, d, J 6.1 Hz), 1.53 (1 H, m), 2.09 (1 H, m), 2.17-2.40 (2 H, m), 4.21 (1 H, m) and 4.46 (1 H, dd, J 8.9, 4.7 Hz). [Mass spectrum: +ve ion (ammonia) MNH4+ (148)].

Provenance & Evidence