تفاعل #1178404
ord-5da48be7b3734a138d2b88df3f2962df
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىequipped
- 2درجة الحرارةwith reflux condenser and overhead stirrer
- 3درجة الحرارةthe mixture was heated
- 4درجة الحرارةat reflux for 4 hours
- 5درجة الحرارةAfter cooling
- 6أخرىthe solvents were removed under reduced pressure
- 7أخرىthe residual thionyl chloride was removed by three evaporations
- 8أخرىThe product was recrystallized from 1:4 toluene
- 9أخرىhexane to give 988 g (91% yield)
- 10أخرىafter drying in a vacuum oven
- 11أخرىThe 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.