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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 1-(4-Bromophenoxy)heptane | HCID 599102 | — |
| Reactant | trans-N,N'-dimethyl-1,2-cyclohexanediamine | HCID 2733821 | — |
| Reactant | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl 4-(4-(heptyloxy)phenyl)-3-oxopiperazine-1-carboxylate | HCID 86689683 | 93.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187522B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-dcd3558b6e084ea686fa3d024fe136ba |
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| Source note | uspto-grants-2015_11 |
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