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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390552Generated: October 25, 2026

Triethylamine → Tert-butyl 4-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2390552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
ReactantTert-butyl 4-(3-(4-bromophenyl)propyl)piperazine-1-carboxylateHCID 67025512—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 4-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propyl)piperazine-1-carboxylateHCID 67026379—

Reaction Steps

To a stirred solution of tert-butyl 4-(3-(4-bromophenyl)propyl)piperazine-1-carboxylate (2.4 g, 6.26 mmol) in acetonitrile (12 ml) was added triethylamine (2.62 ml, 18.78 mmol) and Pd-118 (0.122 g, 0.19 mmol). Reaction mixture was stirred at RT under nitrogen for 10 min. 4,4,5,5-Tetramethyl-1,3,2-dioxaborolane (1.363 ml, 9.39 mmol) added and reaction mixture heated to 80° C. for 1 h. The reaction mixture was evaporated to dryness and redissolved in EtOAc and washed with water and saturated brine. The organic was dried over magnesium sulfate, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography using Isco Companion, 100 g silica column, elution gradient 40 to 100% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford sub-title compound as a brown oil. Yield: 0.9 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273774B2
Source datasetuspto-grants-2012_09
ORD IDord-1a34645d83d54969bd648f89a6326254
Source noteuspto-grants-2012_09