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Hydrazine hydrate (1:1) → HCID 19021158、化合物

HRID 1108920
ノート
印刷プレビュー

反応式

HRID 1108920 の反応式
[N+:1]([C:4]1[CH:9]=[C:8]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[CH:7]=[CH:6][C:5]=1[OH:16])([O-])=O.O.NN>C(O)C>[NH2:1][C:4]1[CH:9]=[C:8]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[CH:7]=[CH:6][C:5]=1[OH:16]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 190211464-Hexyl-2-nitrophenol

生成物 1

HCID 19021158HCID 19021158、化合物収率 81.9%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
70 °C

実験手順

In a 50 ml-three-necked flask, 1.10 g (4.93 mM) of 2-nitro-4-hexylphenol, 0.30 g of activated carbon, 0.02 g of FeCl3.6H2O and 5 ml of ethanol were placed and heated to 55°-70° C. under stirring. To the mixture, 1.5 ml of 80% hydrazine hydrate was gradually added dropwise and heated to 70° C., followed by stirring for 30 min at 70°-75° C. After the reaction, the reaction mixture was filtered under heating to remove the activated carbon and the filtrate was poured into water to precipitate a crystal. The crystal was recovered by filtration, followed by drying under reduced pressure to obtain 0.78 g of 2-amino-4-hexylphenol (yield: 81.9%).

後処理

  1. temperatureheated to 55°-70° C.
  2. stirringby stirring for 30 min at 70°-75° C
  3. customAfter the reaction
  4. filtrationthe reaction mixture was filtered
  5. temperatureunder heating
  6. customto remove the activated carbon
  7. additionthe filtrate was poured into water
  8. customto precipitate a crystal
  9. filtrationThe crystal was recovered by filtration
  10. customby drying under reduced pressure

出典と根拠

ORDレコード
ord-2b501b930cc3497f9776814bda383a26
出典データセット
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05318720

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート