Hydrochloric Acid → HCID 178427293, Verbindung

HRID 1725118

Reaktionsgleichung

Reaktionsgleichung von HRID 1725118
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[CH:13]=[C:12]([OH:14])[N:11]([CH3:15])[N:10]=1.[OH-].[Na+].[CH2:18]=O.[C:20]1([CH3:29])[CH:25]=[CH:24][C:23]([S:26]([O-:28])=[O:27])=[CH:22][CH:21]=1.[Na+].Cl>C(O)C.O>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[C:13]([CH2:18][S:26]([C:23]2[CH:24]=[CH:25][C:20]([CH3:29])=[CH:21][CH:22]=2)(=[O:28])=[O:27])=[C:12]([OH:14])[N:11]([CH3:15])[N:10]=1

Komponenten

8

Versuchsvorschrift

3-(2,4-Dichlorophenyl)-5-hydroxy-1-methylpyrazole (1.3 g (5 mmol)) synthesized in Reference Example 6 and 0.3 g (7.5 mmol) of sodium hydroxide were dissolved in 5 mL of ethanol. While stirring the resulting solution at room temperature, 1.0 g (11 mmol) of a 35% formalin solution was added dropwise thereto, followed by stirring at the same temperature for 1 hour. Subsequently, 0.9 g (5 mmol) of sodium p-toluenesulfinate was charged thereto at room temperature, and the obtained mixture was stirred for 2 hours. After the reaction, 2.5 g (25 mmol) of 35% hydrochloric acid was added dropwise thereto, 15 mL of water was further added, and the precipitated crystal was collected by filtration, washed twice with 10 mL of water and dried by a hot air drier to obtain 2.1 g (yield: 90.3%) of the title compound as a pale yellow crystal.

Aufarbeitung

  1. stirringby stirring at the same temperature for 1 hour
  2. stirringat room temperature, and the obtained mixture was stirred for 2 hours
  3. additionwas added dropwise
  4. filtrationthe precipitated crystal was collected by filtration
  5. washwashed twice with 10 mL of water
  6. customdried by a hot air drier

Quellen und Nachweise

ORD-Eintrag
ord-68e6cd9d584143c7b9540d5fca4b52d2
Quelldatensatz
uspto-grants-2009_02
Patentnummer
US07488831B2

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