Ethyl bromoacetate → HCID 21790152, Verbindung

HRID 2164336Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2164336
[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-9d1196acfee4444ca22747546903152b
Quelldatensatz
uspto-grants-1985_03
Patentnummer
US04503236

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