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Potassium Hydroxide → 2,6-Dichloro-3-nitrobenzene-1-sulfonyl chloride

HRID 1840329
ノート
印刷プレビュー

反応式

HRID 1840329 の反応式
[OH-].[K+].O.O.[Cl:5][C:6]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][CH:9]=[C:8]([Cl:15])[C:7]=1[S:16]([OH:19])(=O)=[O:17].P(Cl)(Cl)(Cl)(Cl)[Cl:21].O=P(Cl)(Cl)Cl>CO>[Cl:5][C:6]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][CH:9]=[C:8]([Cl:15])[C:7]=1[S:16]([Cl:21])(=[O:19])=[O:17]
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 14797Potassium HydroxideHCID 24813Phosphorus oxychlorideHCID 24819Phosphorus pentachlorideHCID 86587416HCID 86587416、化合物

生成物 1

HCID 234477722,6-Dichloro-3-nitrobenzene-1-sulfonyl chloride収率 79%

試薬・触媒・溶媒 1

HCID 887Methanol
溶媒

実験手順

Potassium hydroxide (11.54 g, 0.206 mol) was added to a solution of 2,6-dichloro-3-nitrobenzenesulfonic acid dihydrate (37.38 g, 0.137 mol) in MeOH (500 mL) and the reaction was allowed to stir at room temperature for 14 hr. The reaction mixture was concentrated and the resulting solid was dried in vacuo overnight. To this was added PCl5 (29.60 g, 0.142 mol) followed by POCl3 (400 mL) and the mixture was refluxed overnight. The reaction was then cooled to room temperature and concentrated. The resulting mixture was taken up in EtOAc and chilled in an ice bath. Ice chunks were slowly added to the reaction mixture to quench any leftover PCl5. When bubbling ceased, water was added and the reaction mix was extracted with EtOAc. The organic layer was dried (MgSO4) and concentrated to yield 2,6-Dichloro-3-nitrobenzenesulfonyl chloride (31.4 g, 79%).

後処理

  1. concentrationThe reaction mixture was concentrated
  2. customthe resulting solid was dried in vacuo overnight
  3. temperaturethe mixture was refluxed overnight
  4. temperatureThe reaction was then cooled to room temperature
  5. concentrationconcentrated
  6. temperaturechilled in an ice bath
  7. additionIce chunks were slowly added to the reaction mixture
  8. customto quench any leftover PCl5
  9. customWhen bubbling
  10. additionwater was added
  11. additionthe reaction mix
  12. extractionwas extracted with EtOAc
  13. dry with materialThe organic layer was dried (MgSO4)
  14. concentrationconcentrated

出典と根拠

ORDレコード
ord-3c31329a420e42e59156ac08018110f9
出典データセット
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06680317B2

反応ノート

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