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Urea → (2,3-Difluorophenyl)hydrazine

HRID 1789232
ノート
印刷プレビュー

反応式

HRID 1789232 の反応式
[F:1][C:2]1[C:8]([F:9])=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].[N:10]([O-])=O.[Na+].NC(N)=O>O.Cl>[F:1][C:2]1[C:8]([F:9])=[CH:7][CH:6]=[CH:5][C:3]=1[NH:4][NH2:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 1176UreaHCID 782782,3-DifluoroanilineHCID 23668193Sodium Nitrite

生成物 1

HCID 12891832(2,3-Difluorophenyl)hydrazine収率 98.5%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒2 回HCID 962Water溶媒

実験手順

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

In each of two flasks, 775 mmol (100 g) of 2,3-difluoroaniline were added to 2 L of concentrated hydrochloric acid at -15° C. and treated dropwise with a solution of 852 mmol (58.9 g) of sodium nitrite in 500 mL of water. Ten minutes after the addition, the reaction was treated with 930 mmol (55.8 g) of urea. This was followed by rapid addition of a solution of stannous chloride dihydrate (968 mmol, 220 g) in 700 mL of concentrated hydrochloric acid precooled to -50° C. After 20 minutes, the solid from both reactions was filtered and combined. It was put into 3 L of 1M NaOH (aq) and extracted with 4×500 mL of ether. The extracts were combined, dried over MgSO4 and concentrated to afford 110 g of 2,3-difluorophenylhydrazine (763 mmol, 49%).

後処理

  1. additionTen minutes after the addition
  2. customprecooled to -50° C
  3. filtrationthe solid from both reactions was filtered
  4. extractionextracted with 4×500 mL of ether
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-1ce98538753c4615be5ca5b3ffca31d6
出典データセット
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04687860

反応ノート

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