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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043483Generated: October 31, 2026

1-Piperidinecarboxaldehyde → Tert-butyl 4-formylpyridin-3-ylcarbamate

https://huagongshe.com/reaction/1043483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PiperidinecarboxaldehydeHCID 17429—
Reactant3-(Boc-amino)pyridineHCID 10932321—
ReactantHCID 178418306HCID 178418306—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-formylpyridin-3-ylcarbamateHCID 1417712660.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of tert-butyl pyridin-3-ylcarbamate (17.7 g, 91.1 mmol) in THF (300 mL) was cooled to −78° C. and treated with 1.70 M tert-butyllithium in pentane (129 mL). Upon completion of the addition, the reaction was stirred at −78° C. for an additional 15 min and then at −20° C. for 1.5 h. 1-piperidinecarboxaldehyde (30.4 mL, 0.273 mol) was added while the temperature was maintained below at −15° C., and then the mixture was allowed to stir at room temperature overnight. The solution was cooled to 0° C. and was quenched by the addition of 1 M HCl to bring the pH to 2. Solid Na2CO3 was then added to adjust the pH to 7. The solution was extracted with ethyl acetate three times, and the combined organic solutions were washed with water (3×) and brine. The organic layer was dried, filtered, and volatiles evaporated. The residue was purified by silica gel chromatography (50% ethyl acetate/hexanes) to give the desired product as a yellow solid (12.2 g, 60%). LCMS for C11H15N2O3(M+H)+: m/z=223.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563541B2
Source datasetuspto-grants-2013_10
ORD IDord-a07458a59f644cd7a91ed6ddd3ca6460
Source noteuspto-grants-2013_10