تفاعل #68698

ord-b35a550697104ceb8fa76ba10f219eba

معادلة التفاعل

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
المردود 47.2%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
30°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was heated
  2. 2
    درجة الحرارةto reflux for sixteen hours
  3. 3
    غسيلThe reaction mixture was washed with water (2×500 milliliters)
  4. 4
    تركيزThe organic layer was concentrated under reduced pressure to a yellow solid
  5. 5
    workup.ADDITION1000 milliliters of hexane was added
  6. 6
    درجة الحرارةthe mixture was heated to reflux
  7. 7
    درجة الحرارةThe mixture was cooled
  8. 8
    ترشيحfiltered
  9. 9
    تركيزThe filtrate was concentrated
  10. 10
    أخرىto yield a yellow solid
  11. 11
    أخرىThe yellow solid was recrystallized twice from ethanol

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08529671B2uspto-grants-2013_09