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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077845Generated: October 25, 2026

Potassium Carbonate → Tert-butyl 4-(2-chloro-4-cyanophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2077845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Chloro-4-fluorobenzonitrileHCID 145525—
ProductTert-butyl 4-(2-chloro-4-cyanophenyl)piperazine-1-carboxylateHCID 5832439379%

Reaction Steps

Tert-Butyl piperazine-1-carboxylate (0.931 g, 5 mmol) and 3-chloro-4-fluorobenzonitrile (0.785 g, 5.00 mmol) were combined, K2CO3 (0.898 g, 6.50 mmol) was added and the reaction mixture was stirred at 90° C. for 1d. The mixture was triturated with ethyl acetate (3×5 mL) and the combined organic extracts were filtered. This was concentrated down to about 5-10 mL and subjected to flash column chromatograhy on silica gel (120 g SiO2, hexanes:ethyl acetate 1:0 to 4:1) to afford tert-butyl 4-(2-chloro-4-cyanophenyl)piperazine-1-carboxylate (1.264 g, 3.93 mmol, 79% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 1.42 (s, 9H) 3.00-3.09 (m, 4H) 3.42-3.53 (m, 4H) 7.25 (d, J=8.59 Hz, 1H) 7.77 (dd, J=8.34, 2.02 Hz, 1H) 7.97 (d, J=2.02 Hz, 1H); [M+H] calc'd for C16H20ClN3O2, 322; found, 322.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928105B2
Source datasetuspto-grants-2011_04
ORD IDord-cd70fbc92fab4219a012e09d2f27d413
Source noteuspto-grants-2011_04