Benzene → HCID 12912154, compound

HRID 1980381Notes

Reaction equation

HRID 1980381 reaction equation
C1C=CC=CC=1.C(N(CC)CC)C.[CH3:14][N:15]1[C:19]([OH:20])=[C:18]([C:21](=[O:29])[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[Cl:28])[C:17]([CH3:30])=[N:16]1.[C:31](Cl)(=[O:33])[CH3:32]>O>[CH3:14][N:15]1[C:19]([O:20][C:31](=[O:33])[CH3:32])=[C:18]([C:21](=[O:29])[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[Cl:28])[C:17]([CH3:30])=[N:16]1

Participants

6

Procedure

In a mixture of 20 ml. of benzene and 0.51 g. of triethylamine is dissolved 1.25 g. of 1,3-dimethyl-4-(2-chlorobenzoyl)-5-hydroxypyrazole and 0.4 g. of acetyl chloride is added dropwise at room temperature with stirring. After completion of the dripwise addition, the mixture is stirred at room temperature for 3 hours. After completion of the reaction, water is added to the reaction mixture to dissolve the salts and an organic layer is separated. The organic layer is dried over anhydrous sodium sulfate and the solvent is distilled off. The resulting oily substance is recrystallized from n-hexane to give crude crystalline substance. The substance is recrystallized from methanol to give 1.20 g. of the desired product as colorless prisms melting at 78°-79° C. Yield 82.2%.

Workup

  1. additionIn a mixture of 20 ml
  2. additionAfter completion of the dripwise addition
  3. stirringthe mixture is stirred at room temperature for 3 hours
  4. additionis added to the reaction mixture
  5. dissolutionto dissolve the salts
  6. customan organic layer is separated
  7. dry with materialThe organic layer is dried over anhydrous sodium sulfate
  8. distillationthe solvent is distilled off
  9. customThe resulting oily substance is recrystallized from n-hexane
  10. customto give crude crystalline substance
  11. customThe substance is recrystallized from methanol
  12. customto give 1.20 g

Sources & evidence

ORD record
ord-e6818b688e454aaaa43be59a6a3bac41
Source dataset
uspto-grants-1985_04
Patent number
US04508910

Reaction notes

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