Formaldehyde → (2S)-2-[benzyl(methyl)amino]propanoic acid

HRID 1722618Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1722618
[CH2:1]([NH:8][C@H:9]([C:11]([OH:13])=[O:12])[CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:14]=O>C(O)=O>[CH3:14][N:8]([CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C@H:9]([C:11]([OH:13])=[O:12])[CH3:10]

Komponenten

4

Edukt 2

HCID 712FormaldehydeHCID 723764N-benzyl-L-alanine

Produkt 1

HCID 825998(2S)-2-[benzyl(methyl)amino]propanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 284Formic AcidLösungsmittel

Versuchsvorschrift

The N-benzylalanine (1), (67 g, 0.374 mole) was taken up in formic acid (41 mL, 88%) and formaldehyde (37 mL, 38%) added. The resulting solution was heated on a steam bath for 11/2 hours. After this period the clear solution was cooled and as much of the solvent as possible removed under reduced pressure. Removal of the water was aided by co-evaporation with methanol. To the residual oil was added methanol (200 mL) and the solution diluted with ether yielding the product as a fine white powder, 63.7 g (88%).

Aufarbeitung

  1. temperatureThe resulting solution was heated on a steam bath for 11/2 hours
  2. temperatureAfter this period the clear solution was cooled
  3. customas much of the solvent as possible removed under reduced pressure
  4. customRemoval of the water
  5. additionTo the residual oil was added methanol (200 mL)
  6. additionthe solution diluted with ether yielding the product as a fine white powder, 63.7 g (88%)

Quellen und Nachweise

ORD-Eintrag
ord-19abd6cebd6646319ae21afeff832679
Quelldatensatz
uspto-grants-1989_08
Patentnummer
US04857440

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