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

3-(2-(2,5-Difluorophenyl)hydrazinyl)propanenitrile → HCID 178511141、化合物

HRID 1466577
ノート
印刷プレビュー

反応式

HRID 1466577 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[NH:9][NH:10][CH2:11][CH2:12][C:13]#[N:14]>S(=O)(=O)(O)O.O.S([O-])([O-])(=O)=O.[Fe+3].S([O-])([O-])(=O)=O.S([O-])([O-])(=O)=O.[Fe+3].S([O-])([O-])(=O)=O.[Fe+2]>[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1/[N:9]=[N:10]/[CH2:11][CH2:12][C:13]#[N:14]
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 1

HCID 668471273-(2-(2,5-Difluorophenyl)hydrazinyl)propanenitrile

生成物 1

HCID 178511141HCID 178511141、化合物収率 91%

試薬・触媒・溶媒 3

HCID 24393Ferrous Sulfate触媒HCID 167265Ferric sulfate hydrate触媒HCID 1118Sulfuric Acid溶媒

実験手順

To a solution of 3-(2-(2,5-difluorophenyl)hydrazinyl)propanenitrile (790 mg) in 15 mL of 2N sulfuric acid was added 2.0 g of iron(III) sulfate hydrate. The reaction mixture was stirred at ambient temperature for 30 min as the iron sulfate slowly dissolved and a yellow oil precipitated. The reaction mixture was extracted with ether, and the extracts were washed with water, brine, dried over sodium sulfate, filtered through a plug of silica gel and concentrated to give 710 mg (91%) of (E)-3-((2,5-difluorophenyl)diazenyl)propanenitrile. LCMS (ESI) m+H=196.2. 1H NMR (400 MHz, CDCl3) δ 7.34-7.08 (m, 3H), 4.54-4.31 (m, 2H), 2.99 (t, 2H).

後処理

  1. dissolutionslowly dissolved
  2. customa yellow oil precipitated
  3. extractionThe reaction mixture was extracted with ether
  4. washthe extracts were washed with water, brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered through a plug of silica gel
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-fda8bb9e28b04d598f8243909c36dcef
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08999998B2

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