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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716415Generated: November 1, 2026

Potassium Carbonate → Tert-butyl 4-(4-(heptyloxy)phenyl)-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/716415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIodide IonHCID 30165—
Reactant1-(4-Bromophenoxy)heptaneHCID 599102—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
CatalystCopperHCID 23978—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 4-(4-(heptyloxy)phenyl)-3-oxopiperazine-1-carboxylateHCID 8668968393.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirring solution of 1-bromo-4-(heptyloxy)benzene (447 mg, 1.65 mmol) in dioxane (5 mL) were added tert-butyl 3-oxopiperazine-1-carboxylate (330 mg, 1.65 mmol), copper I iodide (31.4 mg, 0.17 mmol), (1R,2R)—N1,N2-dimethylcyclohexane-1,2-diamine (234 mg, 1.65 mmol) and potassium carbonate (456 mg, 3.30 mmol). The reaction mixture was heated at 120° C. for 16 h. The reaction mixture was passed through a plug of celite, eluted with EA (50 mL). The organics were washed with ammonium chloride (25 mL), water (25 mL) and brine (25 mL) then dried over MgSO4 and concentrated to afford 602 mg (89%) of tert-butyl 4-(4-(heptyloxy)phenyl)-3-oxopiperazine-1-carboxylate. LCMS-ESI (m/z) calculated for C22H34N2O4: 390.5. found 319.0 [M+H]+, tR=2.90 min. (Method 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187522B2
Source datasetuspto-grants-2015_11
ORD IDord-dcd3558b6e084ea686fa3d024fe136ba
Source noteuspto-grants-2015_11