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

HRID 906547
ノート
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反応式

HRID 906547 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

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

生成物 1

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

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8a325f1f03bb417cb75d5c562023b138
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08012988B2

反応ノート

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