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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511065Generated: October 30, 2026

Potassium Iodide → 4-[4-(4-Trifluoromethyl-phenyl)-piperazin-1-yl]-butyric acid ethyl ester

https://huagongshe.com/reaction/511065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant1-(4-(Trifluoromethyl)phenyl)piperazineHCID 121718—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-[4-(4-Trifluoromethyl-phenyl)-piperazin-1-yl]-butyric acid ethyl esterHCID 5857659398%

Reaction Steps

Ethyl-4-bromobutyrate (390 mg, 2.00 mmol) and triethylamine (280 μL; 2.00 mmol) were added to a solution of 1-(4-trifluoromethylphenyl)-piperazine (460 mg; 2.00 mmol) in tetrahydrofuran (3 mL). Potassium iodide (332 mg; 2.00 mmol) was added and the resulting suspension is irradiated in a mono-mode microwave oven for 2 hours at 100° C. The suspension is then diluted with dichloromethane (15 mL) and washed twice with water (5 mL). The organic phase is then dried over sodium sulphate and is concentrated under reduced pressure to afford the desired product (660 mg; 1.96 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096524B2
Source datasetuspto-grants-2015_08
ORD IDord-3760a034e1e54b5895f97400fcb86c3d
Source noteuspto-grants-2015_08