Reacción #1483097

ord-0fd72ae3961e481da85ef8949825dc29

Ecuación de reacción

Cc1ccc(S(=O)(=O)O)cc1
pTSA
CC(C)CC(N)C(=O)O
DL-leucine
CCCCCCCCCCCCO
1-dodecanol
CCCCCCCCCCCCOC(=O)C(N)CC(C)C
43
Rendimiento 102.2%
CCCCCCCCCCCCOC(=O)C(N)CC(C)C
dodecyl 2-amino-4-methylpentanoate
Rendimiento 102.2%

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    Temperaturathe temperature of the reaction mixture was slowly raised
  3. 3
    Temperaturato reflux temperature
  4. 4
    Otrothe water was separated azeotropically
  5. 5
    ConcentraciónThe reaction mixture was concentrated under vacuum
  6. 6
    Lavadowashed with aqueous 5% Na2CO3 (3×50 mL)
  7. 7
    SecadoThe organic layer was dried over Na2SO4
  8. 8
    Concentraciónconcentrated under vacuum

Procedimiento

To a stirred solution of DL-leucine 42 (20 g, 152 mmol) in toluene (400 mL) was added 1-dodecanol 2 (25.56 g, 137.2 mmol) in one lot, followed by pTSA (31.9 g, 167.7 mmol). After addition, the temperature of the reaction mixture was slowly raised to reflux temperature, the water was separated azeotropically, and the reaction mixture was monitored by TLC. The reaction mixture was concentrated under vacuum, the obtained residue was taken in ethyl acetate (200 mL) and washed with aqueous 5% Na2CO3 (3×50 mL) followed by brine solution. The organic layer was dried over Na2SO4 and concentrated under vacuum to afford crude 43 (42 g, yield: 91.9%) as a liquid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08900625B2uspto-grants-2014_12