Ethyl bromoacetate → HCID 21790152, Verbindung

HRID 1982412Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1982412
[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH3:16])[C:8]2[C:13]([C:14]=1[OH:15])=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:5])[CH3:2].Br[CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]>>[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH3:16])[C:8]2[C:13]([C:14]=1[O:15][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:5])[CH3:2]

Komponenten

3

Edukt 2

HCID 7748Ethyl bromoacetateHCID 54696099Ethyl 3-hydroxy-1-methyl-1H-indole-2-carboxylate

Produkt 1

HCID 21790152HCID 21790152, Verbindung

Versuchsvorschrift

Prepared by the procedure described in Example 1 from 3-hydroxy-1-methyl-1H-indole-2-carboxylic acid ethyl ester and ethyl bromoacetate. The crude oil product obtained after evaporation was used for further synthesis without additional purification.

Aufarbeitung

  1. customPrepared by the procedure
  2. customThe crude oil product obtained
  3. customafter evaporation
  4. customwas used for further synthesis without additional purification

Quellen und Nachweise

ORD-Eintrag
ord-d232d72761074da4be734718ed725ba6
Quelldatensatz
uspto-grants-1986_06
Patentnummer
US04596814

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