反应详情

A mixture of 3-tert-butyl-1H-pyrazole-5-carbaldehyde (1.52 g, 10.0 mmol), benzyltriphenylphosphonium bromide (6.50 g, 15.0 mmol), potassium carbonate (2.76 g, 20.0 mmol) and N,N-dimethylformamide (30 mL) was stirred at room temperature for 14 hr. The reaction mixture was poured into 1 N hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layer was concentrated and the residue was purified by silica gel column chromatography (5%-80% ethyl acetate/hexane) to give pale-yellow crystals. The obtained crystals were dissolved in a mixed solvent of ethanol (50 mL) and tetrahydrofuran (50 mL), and 10% palladium-carbon (50% water-containing product, 2.0 g) was added. The mixture was stirred under an atmospheric hydrogen atmosphere for 3 hr. The insoluble material was filtered off, and the filtrate was concentrated to give the title compound (1.90 g, yield 83%) as colorless crystals. 1H NMR (CDCl3) δ: 1.31 (9H, s), 2.90-2.99 (4H, m), 5.89 (1H, s), 7.18-7.33 (5H, m).

1. extractionthe mixture was extracted with ethyl acetate
2. concentrationThe organic layer was concentrated
3. customthe residue was purified by silica gel column chromatography (5%-80% ethyl acetate/hexane)
4. customto give pale-yellow crystals
5. additionwas added
6. stirringThe mixture was stirred under an atmospheric hydrogen atmosphere for 3 hr
7. filtrationThe insoluble material was filtered off
8. concentrationthe filtrate was concentrated