HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 635134Erstellt: 24. Oktober 2026
Hydrochloric Acid → 4-[4-(4-Pentylbicyclo[2.2.2]octyl)phenyl]cyclohexanone
https://huagongshe.com/de/reaction/635134
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 4-Phenylcyclohexanone | HCID 78605 | — |
| Edukt | 1-Bromo-4-pentylbicyclo[2.2.2]octane | HCID 12534977 | — |
| Katalysator | Iron chloride (FeCl3) | HCID 24380 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Nitrobenzene | HCID 7416 | — |
| Produkt | 4-[4-(4-Pentylbicyclo[2.2.2]octyl)phenyl]cyclohexanone | HCID 21257793 | 69% |
Reaktionsschritte
A solution of 1-bromo-4-pentylbicyclo[2.2.2]octane (6 g, 23 mmol) in sieve-dried nitrobenzene (100 cm3) is added dropwise to a stirred solution of 4-phenylcyclohexanone (3.9 g, 23 mmol) and anhydrous iron(III)chloride (1.2 g, 9 mmol) in sieve-dried nitrobenzene (100 cm3) maintained at 80° C. through the addition and overnight. The cooled solution is added to a small volume of hydrochloric acid and stirred for 20 min. The organic layer is separated off and steam-distilled to yield a solid residue. This is taken up in dichloromethane and dried (MgSO4). The raw product is crystallised from ethanol to yield the desired 4-[4-(4-pentylbicyclo[2.2.2]octyl)phenyl]cyclohexanone (5.4 g, 69%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06187393B1 |
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| Quelldatensatz | uspto-grants-2001_02 |
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| ORD ID | ord-be735ef3d5cf49dcaf2d6850a47c7c20 |
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| Quellennotiz | uspto-grants-2001_02 |
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