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Hydrochloric Acid → N~1~-(4-Azido-2-nitrophenyl)propane-1,3-diamine

HRID 638528
ノート
印刷プレビュー

反応式

HRID 638528 の反応式
[NH2:1][CH2:2][CH2:3][CH2:4][NH2:5].F[C:7]1[CH:12]=[CH:11][C:10]([N:13]=[N+:14]=[N-:15])=[CH:9][C:8]=1[N+:16]([O-:18])=[O:17].O.Cl>C(O)C>[N:13]([C:10]1[CH:11]=[CH:12][C:7]([NH:1][CH2:2][CH2:3][CH2:4][NH2:5])=[C:8]([N+:16]([O-:18])=[O:17])[CH:9]=1)=[N+:14]=[N-:15]
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 4

HCID 313Hydrochloric AcidHCID 4281,3-PropanediamineHCID 962WaterHCID 931211-Fluoro-2-nitro-4-azidobenzene

生成物 1

HCID 12716508N~1~-(4-Azido-2-nitrophenyl)propane-1,3-diamine

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

2.5 ml (30 mM) 1,3-diaminopropane was dissolved in 25 ml ethanol. To this solution, was added a solution of 1.82 g (10 mM) 4-fluoro-3-nitrophenyl azide in 25 ml ethanol. The addition was performed dropwise with stirring. The mixture was stirred at room temperature for 16 hours. After this time, 150 ml of water were added and the pH adjusted to between 1 and 2 with concentrated HCl. This solution was filtered to remove the disubstituted amine, cooled on ice and the product was precipitated by the slow addition of concentrated aqueous ammonia with stirring. The product was collected by filtration of the cold mixture, washed with ice-cold water and dried in vacuo.

後処理

  1. additionThe addition
  2. stirringThe mixture was stirred at room temperature for 16 hours
  3. filtrationThis solution was filtered
  4. customto remove the disubstituted amine
  5. temperaturecooled on ice
  6. customthe product was precipitated by the slow addition of concentrated aqueous ammonia
  7. stirringwith stirring
  8. filtrationThe product was collected by filtration of the cold mixture
  9. washwashed with ice-cold water
  10. customdried in vacuo

出典と根拠

ORDレコード
ord-084583ee2b79404bb86e4065d52346e4
出典データセット
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04562157

反応ノート

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