تفاعل #725871

ord-9a35a9a293284e53bd65a7cdfebdea1d

معادلة التفاعل

O=C(O)c1ccccc1
benzoic acid
O=C(O)c1ccccc1
benzoic acid
OCCc1ccccc1
2-phenylethyl alcohol
O=C(OCCc1ccccc1)c1ccccc1
2-phenylethyl benzoate
المردود 90.0%

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
180°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe system was heated gently
  2. 2
    workup.DISSOLUTIONdissolved
  3. 3
    أخرىThe air was removed with three cycles of evacuation/nitrogen
  4. 4
    درجة الحرارةwas increased to ca. 200 rpm
  5. 5
    أخرىthe nitrogen sparge
  6. 6
    درجة الحرارةAfter a 1-h hold, the temperature was increased to 190° C. for 1 h
  7. 7
    درجة الحرارةThe temperature was increased to 210° C.
  8. 8
    أخرىthe nitrogen sparge
  9. 9
    درجة الحرارةwas increased to 0.5 scfh
  10. 10
    درجة الحرارةAfter a 1-h hold, the temperature was further increased to 220° C. for 1 h
  11. 11
    أخرىfrom which 94.4 g of water (theor. 99.1 g) was separated as the top layer
  12. 12
    درجة الحرارةThe reaction mixture was cooled to room temperature
  13. 13
    workup.ALIQUOTsampled for analysis
  14. 14
    أخرىThe excess 2-phenylethyl alcohol (5.5% by GLC) was removed by vacuum distillation
  15. 15
    workup.WAITThus, after 1 h at 180-190° C.
  16. 16
    workup.ADDITIONActivated carbon (37.3 g, 3% w/w) was added
  17. 17
    درجة الحرارةthe mixture was heated at 75-80° C. under vacuum (50-70 torr) for 1 h
  18. 18
    درجة الحرارةAfter cooling to room temperature
  19. 19
    ترشيحfiltration through Celite®

الإجراء التجريبي

A 2-L, 4-neck round bottom flask, fitted with a thermometer, mechanical stirrer, nitrogen inlet tube and Liebig condenser/receiving flask, was charged with 671.7 g (5.50 mol, 1.00 equiv) of benzoic acid, 806.3 g (6.60 mol, 1.20 equiv) of 2-phenylethyl alcohol, and 1.25 g (0.1% w/w) of Fascat 2001®. The system was heated gently with slow stirring (<50 rpm) until the benzoic acid dissolved. The air was removed with three cycles of evacuation/nitrogen fill using a mechanical vacuum pump (50-100 torr). The rate of stirring was increased to ca. 200 rpm, the nitrogen sparge was set at 0.2 scfh, and the reaction mixture was heated to 180° C. After a 1-h hold, the temperature was increased to 190° C. for 1 h and then to 200° C. for 1 h. The temperature was increased to 210° C. and the nitrogen sparge was increased to 0.5 scfh. After a 1-h hold, the temperature was further increased to 220° C. for 1 h. The total amount of distillate was 159.2 g, from which 94.4 g of water (theor. 99.1 g) was separated as the top layer. The reaction mixture was cooled to room temperature and sampled for analysis. The acid number was 1.10 mg KOH/g (99.7% conversion) and the APHA color was 115. The excess 2-phenylethyl alcohol (5.5% by GLC) was removed by vacuum distillation. Thus, after 1 h at 180-190° C. and 20 torr (0.5 scfh nitrogen sweep), the residual 2-phenylethyl alcohol was <0.05% by GLC and the APHA color was 222. Activated carbon (37.3 g, 3% w/w) was added, and the mixture was heated at 75-80° C. under vacuum (50-70 torr) for 1 h. After cooling to room temperature, filtration through Celite® gave 1100 g (90%) of 2-phenylethyl benzoate. The APHA color was 20, the acid number was 0.14 mg KOH/g, the saponification number was 246 mg KOH/g (theor. 248), and the residual tin was <10 ppm.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07691363B2uspto-grants-2010_04