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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067887Generated: October 31, 2026

Pyridine → Ethyl 4-benzyl-2-(trifluoromethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2067887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
Reactant1-Benzyl-3-(trifluoromethyl)piperazineHCID 53407170—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-benzyl-2-(trifluoromethyl)piperazine-1-carboxylateHCID 68748441—

Reaction Steps

To a solution of 1-benzyl-3-(trifluoromethyl)piperazine 34a (1.0 mmol) and pyridine (1.1 mmol) in DCM (5 mL), is added ethyl chloroformate (1.1 mmol). The resulting mixture is stirred at rt for 1 h. After the reaction is complete, the reaction mixture is diluted with DCM (15 mL) and washed with water. The organic layer is separated, dried over Na2SO4, filtered, and concentrated to afford ethyl 4-benzyl-2-(trifluoromethyl)piperazine-1-carboxylate 34b, which is used without purification. MS (m/z) (M+1)+: 317.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293757B2
Source datasetuspto-grants-2012_10
ORD IDord-905d12cf53f54e80aecdd4a690d6e656
Source noteuspto-grants-2012_10