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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Reactant | 1,2-Diaminocyclohexane, trans- | HCID 43806 | — |
| Reactant | Tert-butyl 1-(4-bromophenyl)cyclopropanecarboxylate | HCID 66661920 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl1-[4-(2-oxo-pyrrolidin-1-yl)phenyl]cyclopropanecarboxylate | HCID 66661882 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776874B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-b313cd33f1874e178117e55a775d6495 |
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| Source note | uspto-grants-2010_08 |
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