4-Bromobenzohydrazide → 2-(4-Bromophenyl)-5-methyl-1,3,4-oxadiazole

HRID 1992541

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HRID 1992541 반응식
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([NH:8][NH2:9])=[O:7])=[CH:4][CH:3]=1.CO[C:14](OC)(N(C)C)[CH3:15].O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CN(C)C=O>[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]2[O:7][C:14]([CH3:15])=[N:9][N:8]=2)=[CH:4][CH:3]=1

참가 물질

5

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온도
60 °C

실험 절차

4-Bromo-benzoic acid hydrazide (12.90 g, 60 mmol) and N,N-dimethylacetamide dimethyl acetal (12 mL, 82.0 mmol) were dissolved in N,N-dimethylformamide (100 mL) and the solution heated to 60° C. for 2 hours. The solution was concentrated in vacuo and the residue taken up in toluene (80 mL) and treated with para-toluenesulfonic acid monohydrate (200 mg, 1.50 mmol). The mixture was heated to reflux for 2 hours, allowed to cool, and the product crystallised from the solution and was collected by filtration. The crude product was washed with ether and dried in vacuo to yield a white solid. The filtrate was concentrated in vacuo and the residue combined with the white solid, dissolved in toluene (50 mL) and treated with para-toluenesulfonic acid monohydrate (100 mg, 0.75 mmol). The mixture was heated to reflux for 3 hours, allowed to cool and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with pentane:ethyl acetate 80:20 to 40:60 to yield the title product, 12.00 g.

후처리

  1. concentrationThe solution was concentrated in vacuo
  2. temperatureThe mixture was heated
  3. temperatureto reflux for 2 hours
  4. temperatureto cool
  5. customthe product crystallised from the solution
  6. filtrationwas collected by filtration
  7. washThe crude product was washed with ether
  8. customdried in vacuo
  9. customto yield a white solid
  10. concentrationThe filtrate was concentrated in vacuo
  11. dissolutiondissolved in toluene (50 mL)
  12. temperatureThe mixture was heated
  13. temperatureto reflux for 3 hours
  14. temperatureto cool
  15. concentrationconcentrated in vacuo
  16. customThe residue was purified by column chromatography on silica gel eluting with pentane:ethyl acetate 80:20 to 40:60

출처 및 근거

ORD 기록
ord-35e244821bf246f5b6758f3ca0a93f3b
출처 데이터셋
uspto-grants-2010_01
특허 번호
US07649003B2

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