تفاعل #1178404

ord-5da48be7b3734a138d2b88df3f2962df

معادلة التفاعل

O=C(O)c1ccc(C(=O)c2ccccc2)cc1
4-Benzoylbenzoic acid
O=S(Cl)Cl
thionyl chloride
Cc1ccccc1
toluene
O=C(Cl)c1ccc(C(=O)c2ccccc2)cc1
4-Benzoylbenzoyl Chloride
المردود 91.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىequipped
  2. 2
    درجة الحرارةwith reflux condenser and overhead stirrer
  3. 3
    درجة الحرارةthe mixture was heated
  4. 4
    درجة الحرارةat reflux for 4 hours
  5. 5
    درجة الحرارةAfter cooling
  6. 6
    أخرىthe solvents were removed under reduced pressure
  7. 7
    أخرىthe residual thionyl chloride was removed by three evaporations
  8. 8
    أخرىThe product was recrystallized from 1:4 toluene
  9. 9
    أخرىhexane to give 988 g (91% yield)
  10. 10
    أخرىafter drying in a vacuum oven
  11. 11
    أخرىThe final compound was stored for use in the preparation of a monomer

الإجراء التجريبي

4-Benzoylbenzoic acid (BBA), 1.0 kg (4.42 moles), was added to a dry 5 liter Morton flask equipped with reflux condenser and overhead stirrer, followed by the addition of 645 ml (8.84 moles) of thionyl chloride and 725 ml of toluene. Dimethylformamide, 3.5 ml, was then added and the mixture was heated at reflux for 4 hours. After cooling, the solvents were removed under reduced pressure and the residual thionyl chloride was removed by three evaporations using 3×500 ml of toluene. The product was recrystallized from 1:4 toluene:hexane to give 988 g (91% yield) after drying in a vacuum oven. Product melting point was 92-94° C. Nuclear magnetic resonance (NMR) analysis (1H NMR (CDCl3)) was consistent with the desired product: aromatic protons 7.20-8.25 (m, 9H). All chemical shift values are in ppm downfield from a tetramethylsilane internal standard. The final compound was stored for use in the preparation of a monomer used in the synthesis of Compound III.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08129159B2uspto-grants-2012_03