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Phosphorus oxychloride → 2,3-Dichloro-5-iodopyridine

HRID 462818
ノート
印刷プレビュー

反応式

HRID 462818 の反応式
[Cl:1][C:2]1[C:3](O)=[N:4][CH:5]=[C:6]([I:8])[CH:7]=1.P(Cl)(Cl)(Cl)(Cl)[Cl:11].O=P(Cl)(Cl)Cl>C(Cl)Cl>[Cl:11][C:3]1[C:2]([Cl:1])=[CH:7][C:6]([I:8])=[CH:5][N:4]=1
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

5

反応物 3

HCID 24813Phosphorus oxychlorideHCID 24819Phosphorus pentachlorideHCID 178517798HCID 178517798、化合物

生成物 1

HCID 218928742,3-Dichloro-5-iodopyridine収率 64%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
130 °C

実験手順

A 100 ml 3-necked round bottom flask, fitted with a condenser topped with a N2 inlet, a mechanical stirrer and a thermometer, was charged with 17.2 g (0.0673 mole) of 3-chloro-2-hydroxy-5-iodopyridine, 14.85 g (0.0713 mole) of PCl5, and 1 ml (1.68 g; 0.0109 mole) of POCl3. The reaction mixture, containing solids, was slowly stirred and slowly heated to 130° C. The reaction mixture was stirred under N2 for 5 hours after which it was cooled to room temperature and allowed to stand overnight. The reaction mixture was cautiously poured into crushed ice and allowed to stand for 1 hour. Methylene chloride (200 ml) was added to the reaction mixture to dissolve the solids present in it. The layers was separated and the organic phase was washed with dilute base, water and saturated NaCl. After drying over anhydrous MgSO4 and filtration, the solvent was evaporated leaving 11.8 g of a yellow solid. The solid was recrystallized from methanol resulting in 6.60 g of solid that had spectral and physical properties identical to the product obtained in Example 1, STEP D.

後処理

  1. customA 100 ml 3-necked round bottom flask, fitted with a condenser
  2. customtopped with a N2 inlet, a mechanical stirrer
  3. additionThe reaction mixture, containing solids
  4. stirringThe reaction mixture was stirred under N2 for 5 hours after which it
  5. temperaturewas cooled to room temperature
  6. additionThe reaction mixture was cautiously poured
  7. custominto crushed ice
  8. waitto stand for 1 hour
  9. dissolutionto dissolve the solids present in it
  10. customThe layers was separated
  11. washthe organic phase was washed
  12. additionwith dilute base, water and saturated NaCl
  13. dry with materialAfter drying over anhydrous MgSO4 and filtration
  14. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-082aafd763bd47a08e2e03f7ceada57f
出典データセット
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04517368

反応ノート

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