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Ammonium formate → 3-[(E)-2-(3-aminophenyl)vinyl]-5-bromopyridine

HRID 1953404
ノート
印刷プレビュー

反応式

HRID 1953404 の反応式
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6](/[CH:8]=[CH:9]/[C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([N+:16]([O-])=O)[CH:11]=2)[CH:7]=1.C([O-])=O.[NH4+]>C(O)C.O.[Fe]>[NH2:16][C:12]1[CH:11]=[C:10](/[CH:9]=[CH:8]/[C:6]2[CH:5]=[N:4][CH:3]=[C:2]([Br:1])[CH:7]=2)[CH:15]=[CH:14][CH:13]=1
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 2

HCID 2723923Ammonium formateHCID 232981253-bromo-5-[(E)-2-(3-nitrophenyl)vinyl]pyridine

生成物 1

HCID 232980903-[(E)-2-(3-aminophenyl)vinyl]-5-bromopyridine収率 71.3%

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

A mixture of 3-bromo-5-[(E)-2-(3-nitrophenyl)vinyl]pyridine (5.55 g), iron powder (3.05 g) and ammonium formate (5.73 g) in ethanol (90 ml) and water (30 ml) was stirred at 90pbC. for 30 minutes. The mixture was filtered while hot. The filtrate was added to sodium bicarbonate solution and extracted with ethyl acetate twice. The combined organic solution was washed with sodium bicarbonate solution and brine, dried over magnesium sulfate and concentrated to give 3-[(E)-2-(3-aminophenyl)vinyl]-5-bromopyridine (3.57 g).

後処理

  1. filtrationThe mixture was filtered while hot
  2. additionThe filtrate was added to sodium bicarbonate solution
  3. extractionextracted with ethyl acetate twice
  4. washThe combined organic solution was washed with sodium bicarbonate solution and brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-42dfc52151bd4790bacaafcbd35d61f8
出典データセット
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06117875

反応ノート

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