Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Stearyl Alcohol | HCID 8221 | — |
| Edukt | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 11200948 | HCID 11200948 | 52,2% |
Reaktionsschritte
Under a nitrogen atmosphere, a mixture of 1-octadecanol (36 grams, 210 mmol), pyridine (20 milliliters), and dichloromethane (500 milliliters) was heated to reflux. The alcohol dissolved and the solution was allowed to cool 5° C. 4-Nitrobenzoyl chloride (39.0 grams, 210 mmol) was added in portions over a twenty minute period. The reaction mixture was heated to reflux for sixteen hours. The reaction mixture was washed with 250 milliliters of water. The aqueous layer was washed with 250 milliliters of dichloromethane. The organic layers were combined and concentrated under reduced pressure to a light tan solid. Added 500 milliliters of hexane and heated to reflux. A white precipitate formed as the solution was cooled to room temperature. Filtered off the white precipitate and concentrated the filtrate to a light tan solid. The solid was recrystallized from ethanol (500 milliliters) to obtain 46 grams of octadecyl 4-nitrobenzoate as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08529671B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-ae0cee8c1a6a4930922007ad5c59d4ac |
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| Quellennotiz | uspto-grants-2013_09 |
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