HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576079Generated: October 25, 2026
Isopropanol → 4-[(E)-2-cyclohexylethenyl]-2-fluoroaniline
https://huagongshe.com/reaction/576079
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 4-Bromo-2-fluoroaniline | HCID 123050 | — |
| Reactant | (2-Cyclohexylvinyl)boronic acid | HCID 6031024 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Catalyst | 1-Iodopropane | HCID 33643 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[(E)-2-cyclohexylethenyl]-2-fluoroaniline | HCID 86707282 | 99.7% |
Reaction Steps
Isopropanol (60 mL) was added to PEPPSI™-IPr catalyst (161 mg, 0.24 mmol) and tert-butoxy potassium (2.65 g, 23.6 mmol) under an argon atmosphere, and the mixture was stirred at room temperature for 15 min. To the reaction mixture were added trans-(2-cyclohexylvinyl)boronic acid (2.00 g, 13.0 mmol) and 4-bromo-2-fluoroaniline (2.24 g, 11.8 mmol) successively and the mixture was stirred at room temperature for 15 hr. Water was added thereto, the mixture was extracted with ethyl acetate, and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure to afford 4-[(E)-2-cyclohexylethenyl]-2-fluoroaniline as a reddish brown oil (2.58 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035059B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-c09a1b39f8f547cabadb0c5a76a78547 |
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| Source note | uspto-grants-2015_05 |
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