HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485078Generated: October 25, 2026
Toluene → 1-Cyclobutyl-4-nitro-2-(trifluoromethyl)benzene
https://huagongshe.com/reaction/1485078
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Cyclobutylboronic acid | HCID 16217845 | — |
| Reactant | 1-Iodo-4-nitro-2-(trifluoromethyl)benzene | HCID 19261778 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Cyclobutyl-4-nitro-2-(trifluoromethyl)benzene | HCID 118113447 | 47.3% |
Reaction Steps
A mixture of 2-iodo-5-nitrobenzotrifluoride (4.62 g), cyclobutylboronic acid (4.15 g), [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride (4.15 g), cesium carbonate (22.6 g), toluene (67.0 mL) and water (33.0 mL) was stirred in a sealed tube at 80° C. for 6 hours. After cooling the reaction mixture to room temperature, extraction was conducted with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate and after removing the desiccant by filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0-94:6) to give 1-cyclobutyl-4-nitro-2-(trifluoromethyl)benzene as a pale yellow oil (1.69 g).
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-a54d827d309a45b0b43407b8db30ef0c |
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| Source note | uspto-grants-2016_08 |
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