Sulfuric Acid → Acenaphtho[1,2-b]quinoxaline-2-sulfonic acid

HRID 605039

Reaktionsgleichung

Reaktionsgleichung von HRID 605039
[S:1](=[O:5])(=O)([OH:3])[OH:2].[CH:6]1[C:15]2[C:16]3[C:25]([C:13]4[C:14]=2[C:9]([CH:10]=[CH:11][CH:12]=4)=[CH:8][CH:7]=1)=[N:24][C:23]1[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=1)[N:17]=3>O>[CH:6]1[C:15]2[C:16]3[C:25]([C:13]4[C:14]=2[C:9]([CH:10]=[CH:11][CH:12]=4)=[CH:8][C:7]=1[S:1]([OH:3])(=[O:5])=[O:2])=[N:24][C:23]1[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=1)[N:17]=3

Komponenten

4

Edukt 2

HCID 1118Sulfuric AcidHCID 136028Acenaphtho[1,2-b]quinoxaline

Produkt 1

HCID 22141823Acenaphtho[1,2-b]quinoxaline-2-sulfonic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

As represented by the following reaction pathway, 30% fuming sulfuric acid (2.1-liter) was added to 300 g of acenaphtho[1,2-b]quinoxaline obtained by synthesis example 1 and the mixture was stirred at room temperature for 48 hours for reaction. While keeping the obtained solution at 40° C. to 50° C., 4.5-liter of ion exchange water was added for dilution, and the resultant was further stirred for 3 hours. The precipitate was filtered to obtain acenaphtho[1,2-b]quinoxaline-2-sulfonic acid as represented by the following formula (d).

Aufarbeitung

  1. customobtained by synthesis example 1
  2. customat 40° C. to 50° C.
  3. stirringthe resultant was further stirred for 3 hours
  4. filtrationThe precipitate was filtered

Quellen und Nachweise

ORD-Eintrag
ord-f550da6208a4400a9ba8ac4dd6d3767a
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07911569B2

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