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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48472Generated: October 29, 2026

Piperidine → 1-Benzyl 3-ethyl (3S)-piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/48472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
ReactantOxolane--water (1/1)HCID 21881883—
Product1-Benzyl 3-ethyl (3S)-piperidine-1,3-dicarboxylateHCID 40634406100%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 1.0 L round-bottom flask was charged with K2CO3 (29.2 g; 171 mmol), piperidine (50 g; 163 mmol), and a 1:1 mixture of THF/H2O (800 mL). A 150 mL addition funnel was placed on the flask and charged with CbzCl (29.2 g, 171 mmol). The flask was cooled to 0° C. and then CbzCl was added dropwise over 5 minutes. The reaction mixture was warmed to 20° C. and stirred for 1 h. The reaction mixture was extracted with EtOAc (500 mL) and the organic layer was washed with water (500 mL), saturated NaCl (500 mL), dried (MgSO4), filtered and concentrated in vacuo. The crude material (49.3 g, 100% yield) was carried on without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703508B2
Source datasetuspto-grants-2004_03
ORD IDord-6b96d61185a74049914794dfc541726d
Source noteuspto-grants-2004_03