Reaction #1483097

ord-0fd72ae3961e481da85ef8949825dc29

Reaction equation

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
Yield 102.2%
CCCCCCCCCCCCOC(=O)C(N)CC(C)C
dodecyl 2-amino-4-methylpentanoate
Yield 102.2%

Reagents

None

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    Temperaturethe temperature of the reaction mixture was slowly raised
  3. 3
    Temperatureto reflux temperature
  4. 4
    Otherthe water was separated azeotropically
  5. 5
    ConcentrationThe reaction mixture was concentrated under vacuum
  6. 6
    Washwashed with aqueous 5% Na2CO3 (3×50 mL)
  7. 7
    DryingThe organic layer was dried over Na2SO4
  8. 8
    Concentrationconcentrated under vacuum

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08900625B2uspto-grants-2014_12