Reaktion #1483097

ord-0fd72ae3961e481da85ef8949825dc29

Reaktionsgleichung

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

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    Temperaturthe temperature of the reaction mixture was slowly raised
  3. 3
    Temperaturto reflux temperature
  4. 4
    Sonstigethe water was separated azeotropically
  5. 5
    EinengenThe reaction mixture was concentrated under vacuum
  6. 6
    Waschenwashed with aqueous 5% Na2CO3 (3×50 mL)
  7. 7
    TrocknenThe organic layer was dried over Na2SO4
  8. 8
    Einengenconcentrated under vacuum

Vorschrift

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.

Quelle

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