HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485050Generated: October 30, 2026
4-Iodobenzaldehyde → 4-Cyclobutylbenzaldehyde
https://huagongshe.com/reaction/1485050
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Iodobenzaldehyde | HCID 96657 | — |
| Reactant | HCID 178419766 | HCID 178419766 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Cyclobutylbenzaldehyde | HCID 57174353 | — |
Reaction Steps
To a mixture of 4-iodobenzaldehyde (500 mg), bis(triphenylphosphine)palladium(II) dichloride (75.6 mg), copper(I) iodide (24.6 mg) and dehydrated tetrahydrofuran (10.0 mL), cyclobutylzinc bromide (0.5 mol/L, solution in tetrahydrofuran, 6.46 mL) was added and the mixture was stirred in a sealed tube at 60° C. for 14 hours. After cooling to room temperature, the precipitate was removed by filtration through Celite (registered trademark). The filtrate was concentrated under reduced pressure and thereafter purified by silica gel column chromatography (n-hexane:ethyl acetate=98:2-90:10) to give the titled compound as a colorless oil (225 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422240B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4768ea2e423a4be787bc226767c737f6 |
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| Source note | uspto-grants-2016_08 |
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