Réaction #586078

ord-db9fe98de9e94fafb985403d8ff18508

Équation de réaction

CCCCCCCCCCCCCCO
1-tetradecanol
c1ccncc1
pyridine
O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-Nitrobenzoyl chloride
CCCCCCCCCCCCCCOC(=O)c1ccc([N+](=O)[O-])cc1
tetradecyl 4-nitrobenzoate

Conditions de réaction

Température
30°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction mixture was heated
  2. 2
    Températureto reflux for sixteen hours
  3. 3
    LavageThe reaction mixture was then washed twice with water (2×500 milliliters)
  4. 4
    ConcentrationThe organic layer was concentrated under reduced pressure to a yellow solid
  5. 5
    workup.ADDITIONOne thousand (1000) milliliters of hexane was added
  6. 6
    Températurethe mixture was heated to reflux
  7. 7
    TempératureThe mixture was cooled
  8. 8
    Concentrationconcentrated
  9. 9
    Autreto yield a yellow solid
  10. 10
    Filtrationthat was filtered
  11. 11
    AutreThe yellow solid was recrystallized twice from ethanol

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07765698B2uspto-grants-2010_08