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Trifluoroacetic acid → 6-Chloroquinoxaline-2,3-dicarbonitrile

HRID 1755703
Notes
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Reaction equation

HRID 1755703 reaction equation
[NH:1]=[C:2]([C:7]#[N:8])[C:3](=[NH:6])[C:4]#[N:5].[Cl:9][C:10]1[CH:15]=[CH:14][C:13](N)=[C:12](N)[CH:11]=1.FC(F)(F)C(O)=O>O>[Cl:9][C:10]1[CH:11]=[C:12]2[C:13](=[CH:14][CH:15]=1)[N:6]=[C:3]([C:4]#[N:5])[C:2]([C:7]#[N:8])=[N:1]2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6422Trifluoroacetic acidHCID 72634-Chloro-1,2-diaminobenzeneHCID 1199242,3-Diiminobutanedinitrile

Product 1

HCID 3038656-Chloroquinoxaline-2,3-dicarbonitrileYield 59.5%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A mixture of 0.5 g (4.7 mmols) of the diiminosuccinonitrile and 0.67 g (4.7 mmols) of 4-chloro-1,2-phenylenediamine was slowly added to 10 ml of trifluoroacetic acid at about 20° C. over a period of 30 minutes, and the resulting mixture was stirred at room temperature for 8 hours and then allowed to stand overnight. To the reaction mixture was added 50 ml of water, and the solid precipitated was filtered and sufficiently washed with water. The solid thus obtained was dried under reduced pressure, followed by a silica gel column chromatography (eluent: hexane/ethyl acetate (75/25)) and then recrystallization from chloroform/ethanol, wherein 0.6 g (59%) of 6-chloro-2,3-dicyanoquinoxaline was obtained as colorless crystals.

Workup

  1. waitto stand overnight
  2. customthe solid precipitated
  3. filtrationwas filtered
  4. washsufficiently washed with water
  5. customThe solid thus obtained
  6. customwas dried under reduced pressure
  7. customrecrystallization from chloroform/ethanol

Sources & evidence

ORD record
ord-e72353d543a74c4ca334f8ffb7ce053b
Source dataset
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05438135

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes