Reaktion #156269

ord-450d4c0fee3549558dbf0a9a1323f99c

Reaktionsgleichung

CCOC(=O)C(=O)Cl
Chloro-oxo-acetic acid ethyl ester
CC(O)CN
1-amino-propan-2-ol
CCN(CC)CC
triethylamine
CCOC(=O)C(=O)NCC(C)O
title compound
Ausbeute 31.0%
CCOC(=O)C(=O)NCC(C)O
Ethyl 2-(2-hydroxypropylamino)-2-oxo-acetate
Ausbeute 31.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with DCM (2×100 mL)
  2. 2
    Waschenwashed with water (2×50 mL) and brine (50 mL)
  3. 3
    Trocknendried over Na2SO4
  4. 4
    Sonstigeevaporated to dryness
  5. 5
    SonstigeThe crude product is purified by silica gel chromatography
  6. 6
    Wascheneluting with hexane:ethyl acetate (3.0:7.0)

Vorschrift

To a stirred solution of 1-amino-propan-2-ol (15.0 g, 199.7 mmol) in DCM (150.0 mL), is added triethylamine (43.30 mL, 299.56 mmol) at 0° C. Chloro-oxo-acetic acid ethyl ester (22.35 mL, 199.7 mmol) is added dropwise to the reaction mixture at 0° C. and the reaction mixture is stirred for 16 hours at room temperature. The mixture is diluted with water (100 mL) at 0° C., extracted with DCM (2×100 mL), washed with water (2×50 mL) and brine (50 mL), dried over Na2SO4, and evaporated to dryness. The crude product is purified by silica gel chromatography, eluting with hexane:ethyl acetate (3.0:7.0) to give the title compound as a pale yellow gel (10.7 g, 31.0%). ESI/MS m/z 176.2 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08822486B2uspto-grants-2014_09