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0 °C

To a solution of meldrums acid (1.68 g, 11.66 mmol) and 4-(2-oxo-ethyl)-piperidine-1-carboxylic acid tert-butyl ester (2.21 g, 9.72 mmol) in dichloromethane (40 mL) was added acetic acid (0.055 mL, 0.972 mmol) and piperidine (0.096 mL, 0.972 mmol). The mixture was heated at reflux for 3 h, and then allowed to attain room temperature. After being diluted with tert-butyl methyl ether, the mixture was washed with NaHCO3 (sat.) and brine. The organic phase was dried, filtered and concentrated. The residue was dissolved in a mixture of EtOH (40 mL) and acetic acid (20 mL). The solution was cooled to 0° C., and NaBH4 (0.554 g, 14.6 mmol) was added in portions after which the solution was allowed to stir for 30 min at rt and then acidified to pH 3 with 1 M HCl. The solution was extracted several times with dichloromethane. The combined organic phases were dried, filtered, concentrated and filtered through a pad of silica gel (dichloromethane). The solvent was evaporated to give 4-[2-(2,2-Dimethyl-4,6-dioxo-[1,3]dioxan-5-yl)-ethyl]-piperidine-1-carboxylic acid tert-butyl ester as a colorless oil (2.30 g, 65%) which solidified on standing.

1. temperatureThe mixture was heated
2. temperatureat reflux for 3 h
3. customto attain room temperature
4. washthe mixture was washed with NaHCO3 (sat.) and brine
5. customThe organic phase was dried
6. filtrationfiltered
7. concentrationconcentrated
8. dissolutionThe residue was dissolved in a mixture of EtOH (40 mL) and acetic acid (20 mL)
9. extractionThe solution was extracted several times with dichloromethane
10. customThe combined organic phases were dried
11. filtrationfiltered
12. concentrationconcentrated
13. filtrationfiltered through a pad of silica gel (dichloromethane)
14. customThe solvent was evaporated