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Acetamide, N-[(dimethylamino)methylidene]- → N-[(E)-[(2-bromo-5-fluorophenyl)hydrazinylidene]methyl]acetamide

HRID 1664144
ノート
印刷プレビュー

反応式

HRID 1664144 の反応式
Cl.[Br:2][C:3]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][C:4]=1[NH:10][NH2:11].CN([CH:15]=[N:16][C:17](=[O:19])[CH3:18])C>C1COCC1.CC(O)=O>[Br:2][C:3]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][C:4]=1[NH:10]/[N:11]=[CH:15]/[NH:16][C:17](=[O:19])[CH3:18]
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 2

HCID 567145Acetamide, N-[(dimethylamino)methylidene]-HCID 21069774(2-Bromo-5-fluorophenyl)hydrazine hydrochloride

生成物 1

HCID 136094110N-[(E)-[(2-bromo-5-fluorophenyl)hydrazinylidene]methyl]acetamide収率 72.2%

試薬・触媒・溶媒 2

HCID 176Acetic Acid触媒HCID 8028Tetrahydrofuran溶媒

実験手順

Alternatively, to a mixture of (2-bromo-5-fluoro-phenyl)-hydrazine hydrochloride (5.9 g, 28.8 mmol) and N-((dimethylamino)methylene)acetamide (3.30 g, 28.8 mmol) in THF (30 mL) was added 5 drops of HOAc, and the mixture stirred at room temperature under nitrogen for 15 min. The mixture was concentrated in vacuo, and the residue suspended in a mixture of ether (50 mL) and hexanes (50 mL) and the resulting precipitate collected and air-dried to provide 5.7 g of the title compound as an off-white powder. A second crop gave an additional 0.3 g.

後処理

  1. concentrationThe mixture was concentrated in vacuo
  2. additionthe residue suspended in a mixture of ether (50 mL) and hexanes (50 mL)
  3. customthe resulting precipitate collected
  4. customair-dried

出典と根拠

ORDレコード
ord-6363612bd71b49dbb79a559ffe5ae706
出典データセット
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08039458B2

反応ノート

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