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Hydrochloric Acid → Mixture of (1,3-Dimethylpyrazole + 1,5-Dimethylpyrazole)

HRID 1894052
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HRID 1894052 반응식
CNN.COC(OC)CC(=O)C.Cl.[CH3:14][N:15]1[CH:19]=[CH:18][C:17]([CH3:20])=[N:16]1.[CH3:21][N:22]1[C:26]([CH3:27])=[CH:25][CH:24]=[N:23]1>>[CH3:14][N:15]1[CH:19]=[CH:18][C:17]([CH3:20])=[N:16]1.[CH3:21][N:22]1[C:26]([CH3:27])=[CH:25][CH:24]=[N:23]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 313Hydrochloric AcidHCID 6061MethylhydrazineHCID 790961H-Pyrazole, 1,3-dimethyl-HCID 1365021,5-DimethylpyrazoleHCID 2285484,4-Dimethoxy-2-butanone

생성물 1

HCID 67389620Mixture of (1,3-Dimethylpyrazole + 1,5-Dimethylpyrazole)

실험 절차

Methylhydrazine (4.25 mL, 80 mmol) was added to 4,4-dimethoxy-2-butanone (10.63 mL, 80 mmol) with keeping the temperature below 25° C. and the mixture was stirred at r.t. for 16 h. The mixture was poured in aq HCl (6N, 16 mL, 1.2 equiv) with stirring. The MeOH was removed in vacuo and then 50% aqueous NaOH was added until the pH was basic. The mixture was extracted with diethyl ether (3 times). The organic phases were combined, dried (Na2SO4) and concentrated in vacuo to afford a mixture of 1,3-dimethyl-1H-pyrazole and 1,5-dimethyl-1H-pyrazole (4:1 NMR ratio) (7.32 g, 95%) as a yellow syrup which was used in the next step without further purification.

후처리

  1. customthe temperature below 25° C.
  2. stirringwith stirring
  3. customThe MeOH was removed in vacuo
  4. addition50% aqueous NaOH was added until the pH
  5. extractionThe mixture was extracted with diethyl ether (3 times)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated in vacuo
  8. customto afford
  9. customwas used in the next step without further purification

출처 및 근거

ORD 기록
ord-03d196f8408a445a9672b503d5f618bd
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08513268B2

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