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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053524Generated: November 2, 2026

Potassium Carbonate → tert-Butyl 4-(3-phenoxypropyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1053524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(3-phenoxypropyl)piperazine-1-carboxylateHCID 13173628485%

Reaction Steps

To a solution of n-Boc-piperazine (1.08 g, 5.80 mmol) in dry DMF (10 mL) were added anhydrous potassium carbonate (4.01 g, 29.04 mmol) and compound 26 (1.5 g, 6.97 mmol). The reaction mixture was stirred at RT for 8 h. The potassium carbonate was removed by suction filtration and the solvent was removed under reduced pressure. The residue was dissolved with water and extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed by evaporation. The crude product was purified by column chromatography using ethyl acetate:hexane (8:2) to give compound 28 (1.58 g, 85%). 1H NMR (400 MHz, CDCl3) δ 1.39 (s, 9H), 1.92 (s, 2H), 2.36 (s, 4H), 2.48 (s, 2H), 3.39 (s, 4), 3.95 (m, 2), 6.83 (m, 2H), 7.19 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393306B2
Source datasetuspto-grants-2016_07
ORD IDord-fd89a888a43e4f8fb2885c43a4febe79
Source noteuspto-grants-2016_07