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Sulfuric Acid → 5-Amino-1-(o-tolyl)-1H-pyrazole-4-carboxamide

HRID 1434539
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1434539
S(=O)(=O)(O)O.[NH2:6][C:7]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[N:10]=[CH:9][C:8]=1[C:19]#[N:20].[OH-:21].[Na+]>>[NH2:6][C:7]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[N:10]=[CH:9][C:8]=1[C:19]([NH2:20])=[O:21]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 121505575-amino-1-(2-methylphenyl)-1H-pyrazole-4-carbonitrile

Produkt 1

HCID 119839075-Amino-1-(o-tolyl)-1H-pyrazole-4-carboxamide

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

300 ml of 96% strength sulphuric acid are cautiously added to 40.0 g (201.8 mmol) of 5-amino-1-(2-methylphenyl)-1H-pyrazole-4-carbonitrile (Example 9A) while cooling in ice. The mixture is then heated to 40° C. and stirred for 2 hours at this temperature. After cooling, it is poured into 2 l of ice-water and cautiously neutralized with 50% strength sodium hydroxide solution. After extraction with ethyl acetate three times (2 l each time) the combined organic phases are washed with saturated sodium chloride solution and dried over sodium sulphate, and the solvent is distilled off under reduced pressure. 36.0 g (82% of theory) of product (purity >90%) are obtained and are employed without further purification in subsequent reactions.

Aufarbeitung

  1. temperaturewhile cooling in ice
  2. temperatureAfter cooling
  3. extractionAfter extraction with ethyl acetate three times (2 l each time) the combined organic phases
  4. washare washed with saturated sodium chloride solution
  5. dry with materialdried over sodium sulphate
  6. distillationthe solvent is distilled off under reduced pressure
  7. custom36.0 g (82% of theory) of product (purity >90%) are obtained
  8. customare employed without further purification in subsequent reactions

Quellen und Nachweise

ORD-Eintrag
ord-2b6054ec3a9d4ed283db6178851614a4
Quelldatensatz
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07615558B2

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