HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19791Erstellt: 24. Oktober 2026
Potassium Phosphate, Tribasic → 3-Cyclopropyl-4-fluoroaniline
https://huagongshe.com/de/reaction/19791
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Edukt | Tricyclohexylphosphine | HCID 75806 | — |
| Edukt | Cyclopropylboronic acid | HCID 2760897 | — |
| Edukt | 3-Bromo-4-fluoroaniline | HCID 2779286 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 3-Cyclopropyl-4-fluoroaniline | HCID 57416303 | 64% |
Reaktionsschritte
To a solution of 3-bromo-4-fluorophenylamine (synthesized as described in J. Org. Chem. 1981, 46, 2280-2286) (415 mg, 2.18 mmol), cyclopropyl boronic acid (244 mg, 2.84 mmol), potassium phosphate (1.62 g, 7.64 mmol), and tricyclohexyl phosphine (61 mg, 0.22 mmol) in toluene (10 ml) and water (0.5 ml) was added palladium acetate (25 mg, 0.11 mmol) and the reaction mixture was heated to 100° C. overnight. The mixture was then cooled to RT and diluted with water and extracted with ether. The organic phases were combined, washed with brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by flash column chromatography to give 3-cyclopropyl-4-fluorophenylamine (210 mg, 64%). MS (ISP) 152.2 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745477B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-14b57bd0666e45aab253ce6c60b843fa |
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| Quellennotiz | uspto-grants-2010_06 |
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