Nitric Acid → 6-Amino-5-nitropyridine-3-sulfonic acid

HRID 1043243ノート

反応式

HRID 1043243 の反応式
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[N+:12]([O-])([OH:14])=[O:13]>OS(O)(=O)=O>[NH2:1][C:2]1[N:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13]

参加物

4

反応物 2

HCID 944Nitric AcidHCID 4595336-Aminopyridine-3-sulfonic acid

生成物 1

HCID 203244826-Amino-5-nitropyridine-3-sulfonic acid

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

反応条件

温度
50 °C

実験手順

6-Aminopyridine-3-sulfonic acid (20 g) in concentrated H2SO4 (80 mL) was heated at 50° C. until it was completely dissolved. To this solution was added fuming HNO3 dropwise over 20 minutes. The rate of addition was kept slow so that the internal temperature did not exceed 55° C. After the addition was complete, the reaction mixture was heated at 50° C. for 1 hour. After it cooled to room temperature, it was poured into 150 g of ice. The mixture was stirred for another 1 hour. The whole flask was cooled to 0° C., and was kept at 0° C. for another 2 hours. The solid was collected by filtration. The solid was washed with cold 1:1 water/ethanol (20 mL), followed by diethyl ether (10 mL). The solid was dried in a vacuum oven overnight to give the title compound.

後処理

  1. dissolutionwas completely dissolved
  2. additionTo this solution was added
  3. customdropwise over 20 minutes
  4. additionThe rate of addition
  5. customdid not exceed 55° C
  6. additionAfter the addition
  7. temperatureAfter it cooled to room temperature
  8. temperatureThe whole flask was cooled to 0° C.
  9. waitwas kept at 0° C. for another 2 hours
  10. filtrationThe solid was collected by filtration
  11. washThe solid was washed with cold 1:1 water/ethanol (20 mL)
  12. customThe solid was dried in a vacuum oven overnight

出典と根拠

ORDレコード
ord-33b9be365dfe415eade7f6e78a57cd7d
出典データセット
uspto-grants-2013_10
特許番号
US08557983B2

反応ノート

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