Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | 1-Tetradecanol | HCID 8209 | — |
| Edukt | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Tetradecyl 4-nitrobenzoate | HCID 591245 | 47,2% |
Reaktionsschritte
Under a nitrogen atmosphere, a mixture of 1-tetradecanol (96.3 grams, 449 mmol), pyridine (40 milliliters), and dichloromethane (1000 milliliters) was heated to 30° C. 4-Nitrobenzoyl chloride (100 grams, 539 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 water (2×500 milliliters). The organic layer was concentrated under reduced pressure to a yellow solid. 1000 milliliters of hexane was added and the mixture was heated to reflux. The mixture was cooled and filtered. The filtrate was concentrated to yield a yellow solid. The yellow solid was recrystallized twice from ethanol to obtain 77.0 grams of tetradecyl 4-nitrobenzoate as yellow crystals.
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-b35a550697104ceb8fa76ba10f219eba |
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| Quellennotiz | uspto-grants-2013_09 |
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