Reaktion #1483099

ord-218b76e9203544518218aac5b64a18ff

Reaktionsgleichung

CN
mono methyl amine
CCCCCCCCCCCCOC(=O)C(C)Br
59
CCCCCCCCCCCCOC(=O)C(C)Br
dodecyl 2-bromopropanoate
O=C([O-])O.[Na+]
sodium bicarbonate
CCCCCCCCCCCCOC(=O)C(C)NC
60
Ausbeute 82.3%
CCCCCCCCCCCCOC(=O)C(C)NC
dodecyl 2-(methylamino)propanoate
Ausbeute 82.3%

Lösungsmittel

Reaktionsbedingungen

Temperatur
27.5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solid obtained in the reaction mixture
  2. 2
    Filtrationwas filtered under vacuum
  3. 3
    EinengenThe solvent was concentrated
  4. 4
    workup.ADDITIONdiluted with ethyl acetate/water
  5. 5
    workup.STIRRINGstirred for 15 minutes at 25-30° C
  6. 6
    SonstigeThe aqueous and organic layers were separated
  7. 7
    Extraktionthe aqueous layer was extracted with ethyl acetate (2×10 mL)
  8. 8
    WaschenThe combined organic layers were washed with brine solution
  9. 9
    Trocknendried over Na2SO4
  10. 10
    Einengenconcentrated under vacuum

Vorschrift

To a stirred solution of 59 (10 g, 31.2 mmol) in acetonitrile (20 mL) was added sodium bicarbonate (2.62 g, 31.2 mmol) and followed by mono methyl amine (40% in water) (30 mL, 3 vol) at 25-30° C. The reaction mixture was stirred for 3 hour at 25-30° C.; the reaction was monitored by TLC. The solid obtained in the reaction mixture was filtered under vacuum. The solvent was concentrated, diluted with ethyl acetate/water and stirred for 15 minutes at 25-30° C. The aqueous and organic layers were separated, and the aqueous layer was extracted with ethyl acetate (2×10 mL). The combined organic layers were washed with brine solution, dried over Na2SO4 and concentrated under vacuum to afford crude 60 (7 g, yield: 82.3%) as a liquid

Quelle

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