Reacción #725873

ord-0567592156da435590ecbbb4974ec2e8

Ecuación de reacción

COC(=O)c1ccccc1
methyl benzoate
OCCc1ccccc1
2-phenylethyl alcohol
O=C(OCCc1ccccc1)c1ccccc1
2-phenylethyl benzoate
Rendimiento 81.0%

Reactivos

Ninguno

Condiciones de reacción

Temperatura
210°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISTILLATION230 g of distillate was collected
  2. 2
    OtroThe methanol was stripped from the distillate on a Buchi rotary evaporator
  3. 3
    Otrowas collected
  4. 4
    TemperaturaThe batch was heated for 2 h at 210° C. and 2 h at 220° C., whereupon 40 g of distillate
  5. 5
    Otrowas collected
  6. 6
    OtroThe excess 2-phenylethyl alcohol (3.5% by GLC) and methyl benzoate (2.7% by GLC) were removed by vacuum distillation as usual and the product
  7. 7
    workup.ADDITIONwas treated with activated carbon as usual

Procedimiento

The reaction was set up as in Example 2 except that methyl benzoate (748.8 g, 5.50 mol) was used instead of benzoic acid and 671.9 g (5.50 mol) of 2-phenylethyl alcohol was used. After 4 h at 190° C., 230 g of distillate was collected and the reaction mixture was 51% product by GLC. The methanol was stripped from the distillate on a Buchi rotary evaporator and the residue was returned to the reaction flask. The batch was heated for 2 h at 200° C. and 2 h at 210° C., whereupon 170 g of distillate was collected and the reaction mixture was 80% product by GLC. The methanol was stripped from the distillate as before, and the residue was returned to the reaction flask. The batch was heated for 2 h at 210° C. and 2 h at 220° C., whereupon 40 g of distillate was collected and the reaction mixture was 94% product by GLC. The excess 2-phenylethyl alcohol (3.5% by GLC) and methyl benzoate (2.7% by GLC) were removed by vacuum distillation as usual and the product was treated with activated carbon as usual to afford 1000 g (81%) of 2-phenylethyl benzoate. The residual 2-phenylethyl alcohol was 0.30, the APHA color was 40, the acid number was 0.13 mg KOH/g, the saponification number was 245 mg KOH/g, and the residual tin was <10 ppm.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07691363B2uspto-grants-2010_04