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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823830Generated: October 30, 2026

Benzyl chloroformate → HCID 22146749, compound

https://huagongshe.com/reaction/1823830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantN-benzylpiperidin-4-amineHCID 3016528—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 22146749HCID 22146749—

Reaction Steps

Benzyl chloroformate (4.44 g, 26.0 mmol) in ether (10 ml) was added dropwise to an ether (50 ml) solution of N-benzyl-4-piperidinamine (4.50 g, 23.6 mmol) and aqueous sodium hydrogen carbonate (50 ml) at 0° C. After addition was complete the reaction was warmed to room temperature and the layers separated, the organic layer was washed with brine, dried (MgSO4), filtered and the solvent removed under reduced pressure. The residue was dissolved in tetrahydrofuran (80 ml) and lithium aluminium hydride (2.69 g, 70.8 mmol) was added portionwise and the reaction heated under reflux for 12 hours. Upon cooling to 0° C. water (4 ml) was cautiously added followed by 2N sodium hydroxide (4 ml) and the precipitate removed by filtration. The solvent was removed under reduced pressure to yield a yellow oil which was dissolved in ether (100 ml) and hydrogen chloride gas was bubbled through to give a white precipitate. Filtration furnished the title compound as a white solid, 4.30 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041667B1
Source datasetuspto-grants-2006_05
ORD IDord-c5456a5366dc424697347b94d3fe72ed
Source noteuspto-grants-2006_05