ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Hydrogen Peroxide → 2-Chloro-5-fluoropyridine 1-oxide

HRID 1061494
ノート
印刷プレビュー

反応式

HRID 1061494 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][N:3]=1.F[B-](F)(F)F.ClC1C=CC([N+]#N)=CN=1.OO.FC(F)(F)C(O)=[O:28]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][N+:3]=1[O-:28]
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 4

HCID 784Hydrogen PeroxideHCID 6422Trifluoroacetic acidHCID 27828012-Chloro-5-fluoropyridineHCID 22284046HCID 22284046、化合物2 回

生成物 1

HCID 222840302-Chloro-5-fluoropyridine 1-oxide収率 70%

実験手順

2-Chloro-5-fluoropyridine (9), a highly volatile substance, was synthesized from thermolysis of 2-chloro-5-pyridinediazonium tetrafluoroborate (8). Hand, E. S.; Baker, D. C. Synthesis 1989, 905-908. The isolation of 9 by the literature procedure was very complicated, in that it included repeated extractions, repeated distillations, treatment with sulfuric acid and sodium hydroxide, and steam distillation. In our hands, the reported yield of 70% was difficult to obtain after these operations. To improve upon these complicated procedures, following the thermolysis of compound 8, the reaction mixture was directly treated with 50% hydrogen peroxide and trifluoroacetic acid to give 2-chloro-5-fluoropyridine-N-oxide (10), which was easily isolated, with a total yield of 73%. Nitration of 10, followed by catalytic hydrogenation of the resulting 2-chloro-5-fluoro-4-nitropyridine-1-oxide (11) removed the N-oxide function, as well as reduced the nitro group to give the desired 4-amino-2-chloro-5-fluoropyridine (12). N-Oxidation of commercially available 2,5-dichloropyridine (13), followed by nitration and reduction yielded 4-amino-2,5-dichloropyridine (16).

後処理

  1. customSynthesis 1989, 905-908
  2. extractionextractions
  3. distillationwith sulfuric acid and sodium hydroxide, and steam distillation
  4. customto obtain after these operations

出典と根拠

ORDレコード
ord-ad5364f4343448baaa2f991e665466ad
出典データセット
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06960568B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート