Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Tetradecanol | HCID 8209 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tetradecyl 4-nitrobenzoate | HCID 591245 | — |
Reaction Steps
Under a nitrogen atmosphere, a mixture of 1-tetradecanol (96.3 grams, 449 millimoles (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 then washed twice with water (2×500 milliliters). The organic layer was concentrated under reduced pressure to a yellow solid. One thousand (1000) milliliters of hexane was added, and the mixture was heated to reflux. The mixture was cooled and concentrated to yield a yellow solid that was filtered. The yellow solid was recrystallized twice from ethanol to obtain 77.0 grams of tetradecyl 4-nitrobenzoate as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07765698B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-db9fe98de9e94fafb985403d8ff18508 |
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| Source note | uspto-grants-2010_08 |
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