HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046063Generated: October 31, 2026
Cyclopropanecarbonyl chloride → Ethyl 4-cyclopropyl-4-oxobutanoate
https://huagongshe.com/reaction/1046063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | Ethyl 3-iodopropanoate | HCID 10911297 | — |
| Catalyst | Zinc copper couple | HCID 10290809 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Ethyl 4-cyclopropyl-4-oxobutanoate | HCID 24727441 | 70.5% |
Reaction Steps
A mixture of ethyl 3-iodopropanoate (8 g, 35 mmol) and zinc-copper (4.5 g, 70 mmol) in a mixture of benzene (80 mL) and DMA (8 mL) was heated at 60° C. for 4.5 hours under N2. Pd(PPh3)2Cl2 (1.2 g, 1.8 mmol) was added, followed by addition of cyclopropanecarbonyl chloride (3.7 g, 35 mmol). The mixture was stirred at 60° C. for another 30 minutes. The reaction mixture was diluted with ethyl acetate (300 mL), and washed with 1N HCl (50 mL), satd aq NaHCO3 (80 mL) and brine (30 mL). The organic layer was dried over Na2SO4 and concentrated to afford the ethyl 4-cyclopropyl-4-oxobutanoate (4.2 g), which was used for next step directly without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569292B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-7fcecf852594480a9984f12e2cad41b5 |
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| Source note | uspto-grants-2013_10 |
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