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

HRID 1755703
ノート
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反応式

HRID 1755703 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 3038656-Chloroquinoxaline-2,3-dicarbonitrile収率 59.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-e72353d543a74c4ca334f8ffb7ce053b
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05438135

反応ノート

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