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3,5-Diphenyl-4-methylpyrazoline → 4-methyl-3,5-diphenyl-1H-pyrazole

HRID 597582
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HRID 597582 반응식
[C:1]1([C:7]2[NH:8][NH:9][CH:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:11]=2[CH3:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>[Pd].C1(C)C(C)=CC=CC=1>[C:1]1([C:7]2[C:11]([CH3:12])=[C:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[NH:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 706390703,5-Diphenyl-4-methylpyrazoline

생성물 1

HCID 51222584-methyl-3,5-diphenyl-1H-pyrazole

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 7237O-Xylene용매

반응 조건

온도
25 °C

실험 절차

To the crude wet xylene solution of 3,5-diphenyl-4-methylpyrazoline (from B above), is added 1.0 g of 5% palladium on carbon catalyst. The reaction mixture is slowly heated to reflux, and the water removed by azeotropic distillation using a Dean-Stark apparatus (xylene returned to reactor). Refluxing is continued at 145° C for 4 hours. After the four-hour reflux, the reaction mixture is cooled to 25° C, and the combined 5% palladium on charcoal/3,5-diphenyl-4-methylpyrazole filtered off. The solids are slurried in warm acetone to dissolve the 3,5-diphenyl-4-methylpyrazole. The catalyst is then filtered off. Removal of the acetone in vacuo yields 1.5 g of 3,5-diphenyl-4-methylpyrazole. After recrystallization from hot xylene, pure 3,5-diphenyl-4-methylpyrazole having a melting point of 225°-226° C is obtained.

후처리

  1. temperatureThe reaction mixture is slowly heated
  2. temperatureto reflux
  3. customthe water removed by azeotropic distillation
  4. temperatureRefluxing
  5. temperatureAfter the four-hour reflux
  6. filtrationthe combined 5% palladium on charcoal/3,5-diphenyl-4-methylpyrazole filtered off
  7. dissolutionto dissolve the 3,5-diphenyl-4-methylpyrazole
  8. filtrationThe catalyst is then filtered off
  9. customRemoval of the acetone in vacuo

출처 및 근거

ORD 기록
ord-07d324a6cee040949ebd2a36f8660f95
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04014896

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