Methyl chloroglyoxylate → HCID 70816656, Verbindung

HRID 1261780

Reaktionsgleichung

Reaktionsgleichung von HRID 1261780
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:11])[CH2:9][CH3:10])=[C:4]([NH:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:3]=1.Cl[C:20](=[O:25])[C:21]([O:23][CH3:24])=[O:22]>C1(C)C=CC=CC=1>[CH3:24][O:23][C:21](=[O:22])[C:20]([N:12]([C:4]1[CH:3]=[C:2]([Cl:1])[CH:7]=[CH:6][C:5]=1[C:8](=[O:11])[CH2:9][CH3:10])[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1)=[O:25]

Komponenten

4

Edukt 2

HCID 79846Methyl chloroglyoxylateHCID 708166141-(4-Chloro-2-phenylamino-phenyl)-propan-1-one

Produkt 1

HCID 70816656HCID 70816656, VerbindungAusbeute 87,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

A solution of 1-(4-chloro-2-phenylamino-phenyl)-propan-1-one (13.0 g, 50.2 mmol) in toluene (150 mL) at 25° C. was treated with methyl chlorooxoacetate (42.86 g, 350 mmol). The reaction mixture was then heated at 110° C. for 16 h. At this time, the reaction mixture was concentrated in vacuo to afford N-(5-chloro-2-propionyl-phenyl)-N-phenyl-oxalamic acid methyl ester (15.2 g, 87.6%). The material was used without further purification.

Aufarbeitung

  1. concentrationAt this time, the reaction mixture was concentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-a297d1dbe3644a168057496ae77a228f
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08471027B2

Verknüpfte Notizen

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