Nitric Acid → Methyl 2-[(6-chloro-5-nitro-1,2-benzisoxazol-3-yl)oxy]propionate

HRID 259672ノート

反応式

HRID 259672 の反応式
[N+:1]([O-:4])(O)=[O:2].[Cl:5][C:6]1[CH:21]=[CH:20][C:9]2[C:10]([O:13][CH:14]([CH3:19])[C:15]([O:17][CH3:18])=[O:16])=[N:11][O:12][C:8]=2[CH:7]=1>S(=O)(=O)(O)O.CCOCC.C(Cl)Cl>[Cl:5][C:6]1[C:21]([N+:1]([O-:4])=[O:2])=[CH:20][C:9]2[C:10]([O:13][CH:14]([CH3:19])[C:15]([O:17][CH3:18])=[O:16])=[N:11][O:12][C:8]=2[CH:7]=1

参加物

6

実験手順

Nitric acid (70%, 3.0 mL, 47 mmol) is slowly added to a mixture of methyl 2-[(6-chloro-1,2-benzisoxazol-3-yl)oxy]propionate (6.0 g, 23.5 mmol) in concentrated sulfuric acid (50 mL) while maintaining the temperature below 10° C. The reaction mixture is stirred for 1 hour on an ice/water bath and poured onto ice. The resultant aqueous mixture is diluted with ether, stirred for several minutes and the ether is allowed to evaporate overnight. The resultant mixture is filtered to obtain a solid which is dissolved in methylene chloride. The methylene chloride solution is dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a solid which is recrystallized from an ether/hexanes solution to give the title product as a solid, mp 98°-101° C.

後処理

  1. temperaturewhile maintaining the temperature below 10° C
  2. additionpoured onto ice
  3. stirringstirred for several minutes
  4. customto evaporate overnight
  5. filtrationThe resultant mixture is filtered
  6. customto obtain a solid which
  7. dry with materialThe methylene chloride solution is dried over anhydrous sodium sulfate
  8. concentrationconcentrated in vacuo
  9. customto obtain a solid which
  10. customis recrystallized from an ether/hexanes solution

出典と根拠

ORDレコード
ord-e4ae2e5bff3f4b7f92b8ede47a8e3042
出典データセット
uspto-grants-1996_06
特許番号
US05523278

反応ノート

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