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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209167Generated: October 30, 2026

Triethylamine → tert-Butyl 4-(4-bromo-2-cyanophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2209167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-Bromo-2-fluorobenzonitrileHCID 2724900—
SolventDimethyl SulfoxideHCID 679—
Producttert-Butyl 4-(4-bromo-2-cyanophenyl)piperazine-1-carboxylateHCID 5676380880%

Reaction Steps

In a pressure tube, 5-bromo-2-fluorobenzonitrile (2500 mg, 12.5 mmol), tert-butyl piperazine-1-carboxylate (2444.45 mg, 13.12 mmol), triethylamine (5.23 ml, 37.5 mmol) in dimethylsulfoxide (10 ml) were combined and refluxed at 100 C for ovn. The mixture was cooled, and partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The organic phase was dried using sodium sulfate and concentrated. The residue was purified by flash column chromatography on silica gel 5-60% ethyl acetate/hexane to provide a light brown oil, tert-butyl 4-(4-bromo-2-cyanophenyl)piperazine-1-carboxylate (3660 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-f7aeb9dea80e4af889c73bab9a226e2c
Source noteuspto-grants-2016_06