2-Methoxyethanol → CID 101686797

HRID 1156568

Reaktionsgleichung

Reaktionsgleichung von HRID 1156568
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([O-:14])(=[O:13])=[O:12].[Na+:15].[CH3:16][O:17][CH2:18][CH2:19][OH:20].[OH-].[Na+]>[O-2].[O-2].[Mn+4].O>[CH3:16][O:17][CH2:18][CH2:19][O:20][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([O-:14])(=[O:13])=[O:12].[Na+:15]

Komponenten

6

Edukt 3

HCID 80192-MethoxyethanolHCID 14798Sodium HydroxideHCID 70350Benzenesulfonic acid, 2-chloro-5-nitro-, sodium salt (1:1)

Produkt 1

HCID 101686797CID 101686797

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418406HCID 178418406, VerbindungKatalysatorHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

A mixture of 5.2 g of sodium 2-chloro-5-nitrobenzenesulfonate, 0.6 g of manganese dioxide, 15 ml of 2-methoxyethanol, 1 ml of water and 0.95 g of sodium hydroxide was stirred at 75° C. for 40 minutes. After cooling, insoluble products were removed by filtration and the filtrate was poured into 100 ml of isopropyl alcohol. Precipitated crystals were collected by filtration. 4.8 g of sodium 2-(2-methoxyethoxy)-5-nitrobenzenesulfonate was obtained.

Aufarbeitung

  1. temperatureAfter cooling
  2. custominsoluble products were removed by filtration
  3. additionthe filtrate was poured into 100 ml of isopropyl alcohol
  4. customPrecipitated crystals
  5. filtrationwere collected by filtration

Quellen und Nachweise

ORD-Eintrag
ord-b9a3fd1902b74d2ea1620a4ab0f7d0fb
Quelldatensatz
uspto-grants-1982_06
Patentnummer
US04336322

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