Glycine → Methyl (R)-(1-hydroxy-3-methylbutan-2-YL)carbamate

HRID 4939

Reaktionsgleichung

Reaktionsgleichung von HRID 4939
[NH2:1][C@@H:2]([CH2:6][OH:7])[CH:3]([CH3:5])[CH3:4].C(N(CC)CC)C.Cl[C:16]([O:18][CH3:19])=[O:17].NCC(O)=O>C1COCC1>[CH3:19][O:18][C:16]([NH:1][C@@H:2]([CH2:6][OH:7])[CH:3]([CH3:5])[CH3:4])=[O:17]

Komponenten

6

Reaktionsbedingungen

Temperatur
-20 °C

Versuchsvorschrift

39.7 g (0.385 mol) of D-valinol (Aldrich) are dissolved under nitrogen in 500 ml of dry THF. 58.7 ml (0.424 mol) of triethylamine are added, the mixture is cooled to -20° C. and 32.8 ml (0.424 mol) of methyl chloroformate (Aldrich) are added dropwise to the mixture with stirring. The mixture is subsequently stirred at this temperature for 30 minutes and then brought to room temperature. 60 g (0.078 mol) of glycine are added and the mixture is stirred once more for 15 minutes. The precipitate is filtered off with suction, the filtrate is concentrated and the residue is taken up in diethyl ether. The organic phase is washed with 1N HCl, saturated NaHCO3 solution and saturated sodium chloride solution, dried over sodium sulphate, filtered and concentrated, and the residue is dried in a high vacuum.

Aufarbeitung

  1. stirringThe mixture is subsequently stirred at this temperature for 30 minutes
  2. custombrought to room temperature
  3. stirringthe mixture is stirred once more for 15 minutes
  4. filtrationThe precipitate is filtered off with suction
  5. concentrationthe filtrate is concentrated
  6. washThe organic phase is washed with 1N HCl, saturated NaHCO3 solution and saturated sodium chloride solution
  7. dry with materialdried over sodium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customthe residue is dried in a high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-1c632e8d02734363bc97532e616fc30a
Quelldatensatz
uspto-grants-1993_09
Patentnummer
US05242903

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