HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485111Generated: October 31, 2026
Ethanol → 4-Cyclohexen-1-yl-3-fluorobenzonitrile
https://huagongshe.com/reaction/1485111
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 1-Cyclohexenylboronic acid | HCID 3862902 | — |
| Reactant | 3-Fluoro-4-iodobenzonitrile | HCID 24721521 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-Cyclohexen-1-yl-3-fluorobenzonitrile | HCID 118113364 | 78.6% |
Reaction Steps
To a mixture of 3-fluoro-4-iodobenzonitrile (1.53 g), 1-cyclohexen-1-yl-boronic acid (938 mg), bis(triphenylphosphine)palladium(II) dichloride (435 mg) and ethanol (9.75 mL), sodium ethoxide (about 20%, solution in ethanol, 5.75 mL) was added and the mixture was stirred at 90° C. for 15 minutes under irradiation with microwaves. After being cooled to room temperature, the reaction mixture was poured into water and three extractions were conducted with chloroform. The combined organic layers were washed with saturated brine and passed through a phase separator to be concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0-75:25) to give the titled compound as a pale yellow oil (980 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-276de4b7010c42ada4c1c5af8540d4ef |
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| Source note | uspto-grants-2016_08 |
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