Reaction #1483085

ord-51f3d29847f74da5b8d778ed4ea542de

Reaction equation

Cc1ccc(S(=O)(=O)O)cc1
pTSA
CC(N)C(=O)O
DL-alanine
CCCCCCCCCCC(C)O
dodecanol 2
CCCCCCCCCCCCOC(=O)C(C)N
dodecyl 2-aminopropanoate
Yield 110.8%
CCCCCCCCCCCCOC(=O)C(C)N
Dodecyl 2-aminopropanoate
Yield 110.8%

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-alanine 1 (5 g, 56.1 mmol) in toluene (100 mL) was added dodecanol 2 (9.42 g, 50.5 mmol) in one lot, followed by pTSA (11.75 g, 61.7 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 dodecyl 2-aminopropanoate 3 (14.4 g, yield: 100%) as a liquid.

Source

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