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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467539Generated: October 26, 2026

Potassium Carbonate → Tert-butyl 4-(cyclopropanecarbonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1467539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(cyclopropanecarbonyl)piperazine-1-carboxylateHCID 96893673%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of compound tert-butyl piperazine-1-carboxylate (3.725 g, 20 mmol) and potassium carbonate (5.53 g, 40 mmol) in anhydrous dichloromethane (30 mL) was cooled to 0° C., cyclopropanecarbonyl chloride (2.30 g, 22 mmol) was then added dropwise. After the addition, the mixture was stirred at room temperature overnight. The mixture was diluted with dichloromethane (100 mL), washed with 10% citric acid (50 mL), followed by saturated sodium bicarbonate (50 mL), brine (100 mL), dried over anhydrous sodium sulfate, and concentrated to give tert-butyl 4-(cyclopropanecarbonyl)piperazine-1-carboxylate (3.7 g, yield 73%) as a white solid. 1H-NMR (400 MHz, CDCl3) δ (ppm): 0.76-0.81 (m, 2H), 0.98-1.03 (m, 2H), 1.49 (s, 9H), 1.69-1.75 (m, 1H), 3.46-3.48 (m, 4H), 3.63-3.65 (m, 4H); LC-MS (ESI) m/z: 255 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999987B2
Source datasetuspto-grants-2015_04
ORD IDord-0bd281d98b5d4c0fa42453d342c94b10
Source noteuspto-grants-2015_04