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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504289Generated: October 30, 2026

Potassium Carbonate → Tert-butyl1-[4-(2-oxo-pyrrolidin-1-yl)phenyl]cyclopropanecarboxylate

https://huagongshe.com/reaction/504289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-PyrrolidoneHCID 12025—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantTert-butyl 1-(4-bromophenyl)cyclopropanecarboxylateHCID 66661920—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl1-[4-(2-oxo-pyrrolidin-1-yl)phenyl]cyclopropanecarboxylateHCID 66661882—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl 1-(4-bromophenyl)cyclopropanecarboxylate (297.2 mg, 1.0 mmol), 2-oxo-pyrrolidine (1.2 mmol), copper(I) iodide (20.0 mg, 0.1 mmol), (trans)-cyclohexane-1,2-diamine (22.8 mg, 0.2 mmol) and potassium carbonate (300.0 mg, 2.17 mmol) was deaerated under vacuum and then charged with nitrogen. To the mixture was added toluene (2.0 mL). The resulting mixture was heated at 100° C. for overnight. Then ethyl acetate (10 mL) was added to the mixture. The resulting mixture was filtered through a pad of celite, and the solid was washed with additional ethyl acetate. The filtrate was concentrated. The residue was purified by flash chromatography with ethyl acetate/hexane to afford tert-butyl 1-[4-(2-oxo-pyrrolidin-1-yl)phenyl]cyclopropanecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776874B2
Source datasetuspto-grants-2010_08
ORD IDord-b313cd33f1874e178117e55a775d6495
Source noteuspto-grants-2010_08