Diethyl Ether → 3-(((Benzyloxy)carbonyl)amino)-2-methylpropanoic acid

HRID 725655

Reaktionsgleichung

Reaktionsgleichung von HRID 725655
[CH2:1]([O:8][C:9](Cl)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:12][CH2:13][CH:14]([CH3:18])[C:15]([OH:17])=[O:16].C(OCC)C>C1(C)C=CC=CC=1.[OH-].[Na+]>[CH2:1]([O:8][C:9]([NH:12][CH2:13][CH:14]([CH3:18])[C:15]([OH:17])=[O:16])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

6

Edukt 3

HCID 3283Diethyl EtherHCID 10387Benzyl chloroformateHCID 64956Beta-Aminoisobutyric Acid

Produkt 1

HCID 3042743-(((Benzyloxy)carbonyl)amino)-2-methylpropanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1140TolueneLösungsmittelHCID 14798Sodium HydroxideLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of 41.7 ml of chloroformic acid benzyl ester (90%) in toluene is added to 25 g of 3-amino-2(R,S)-methylpropionic acid in 533 ml of 1N sodium hydroxide at 0° C. The reaction mixture is then stirred for 30 minutes at 0° C. After the addition of 400 ml of diethyl ether, the aqueous phase is removed and 140 ml of 4N hydrochloric acid are added. The crude title compound is obtained from the organic phase by extraction with diethyl ether: Rf (dichloromethane/methanol=8:2)=0.41.

Aufarbeitung

  1. customthe aqueous phase is removed
  2. addition140 ml of 4N hydrochloric acid are added

Quellen und Nachweise

ORD-Eintrag
ord-fc361ff62aed4ddea9fce955975be3a7
Quelldatensatz
uspto-grants-1998_01
Patentnummer
US05705658

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