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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205638Generated: November 2, 2026

Triethylamine → Benzyl ethyl piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/2205638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantEthyl nipecotateHCID 98969—
SolventDichloromethaneHCID 6344—
ProductBenzyl ethyl piperidine-1,3-dicarboxylateHCID 1799927197.2%

Reaction Steps

Benzyl chloroformate (Aldrich, cat #:119938) (191 mL, 1.34 mol) was slowly added to a cooled (at 0° C.) mixture of ethyl piperidine-3-carboxylate (Aldrich, cat #:194360) (200 g, 1.27 mol) and triethylamine (266 mL, 1.91 mol) in methylene chloride (1000 mL). The reaction mixture was allowed to gradually warm to ambient temperature and stirred for 3 h. The reaction was quenched by the addition of 1N HCl aq. solution and the product was extracted several times with methylene chloride. The combined extracts were washed with water, saturated aq. NaHCO3, water, brine, dried over MgSO4, filtered and concentrated under reduced pressure to afford the desired product as oil (359.8 g, 97%). LC/MS 292.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371323B2
Source datasetuspto-grants-2016_06
ORD IDord-b11c1067e082435ab8bb1f04b4fbe163
Source noteuspto-grants-2016_06