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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714124Generated: October 26, 2026

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

https://huagongshe.com/reaction/714124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(Chloromethyl)cyclopropaneHCID 80013—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(cyclopropylmethyl)piperazine-1-carboxylateHCID 46743082—

Reaction Steps

1-Tertbutoxycarbonylpiperazine (6a) (1.86 g, 10 mmol) was dissolved in dichloromethane (20 mL), and anhydrous potassium carbonate (829 mg, 6 mmol) was added. The dichloromethane solution of chloromethyl cyclopropane (7a) (1.1 mL, 12 mmol) was added dropwise, and reacted overnight at room temperature, after that, the reaction mixture was washed with water. The water layer was extracted with dichloromethane for twice, the organic phases were combined, washed successively with 50 mL saturated sodium bicarbonate solution and saturated sodium chloride solution for three times, dried with anhydrous sodium sulfate. Column chromatography (petroleum ether:ethyl acetate 2:1) was performed to isolate white solid powder 1-tertbutoxycarbonyl-4-(cyclopropylmethyl)piperazine (7b), 2.01 g white solid (yield 79.0%). ESI-MS m/z calculated for: 240.18. found: 241.05 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187430B2
Source datasetuspto-grants-2015_11
ORD IDord-a7d66c35fb7446b5992eb239529631d2
Source noteuspto-grants-2015_11