Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595015Generated: October 26, 2026

Triethylamine → Tert-butyl 4-(2,5-dicyano-3,4,6-trifluorophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/595015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTetrafluoroterephthalonitrileHCID 15783—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductTert-butyl 4-(2,5-dicyano-3,4,6-trifluorophenyl)piperazine-1-carboxylateHCID 8667174351.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

2,3,5,6-tetrafluoroterephthalonitrile (1 g, 5 mmol) was dissolved in acetone (15 mL) in a 2-necked flask under Nitrogen. A solution of tert-butyl piperazine-1-carboxylate (1.39 g, 7.5 mmol) in water (3 mL) was then added followed by triethylamine (1.01 g, 10 mmol). The solution was heated to 55° C. for 8 h then cooled to rt. The resulting solid was filtered then washed with acetone. The filtrate was concentrated under vacuum and the residue was dissolved again in DCM (30 mL) and washed once with 1M HCl (30 mL) and once with brine (30 mL). The organics were dried over Na2SO4, filtered and the solvent removed in vacuo to give tert-butyl 4-(2,5-dicyano-3,4,6-trifluorophenyl)piperazine-1-carboxylate as a bright yellow solid (0.938 g, 51% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242987B2
Source datasetuspto-grants-2016_01
ORD IDord-0a1c2be596b64a1daf884580694e7663
Source noteuspto-grants-2016_01