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Ethanol → HCID 13882127, Verbindung

HRID 867375
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 867375
[C:1]([C:3]1[N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[CH:9]=2)[N:6]=[CH:5][C:4]=1[C:15]([O:17]CC)=[O:16])#[N:2].[OH-].[K+].C([OH:24])C>O>[C:15]([C:4]1[CH:5]=[N:6][N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[CH:9]=2)[C:3]=1[C:1]([NH2:2])=[O:24])([OH:17])=[O:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 702EthanolHCID 14797Potassium HydroxideHCID 13772971ethyl 5-cyano-1-(3-fluorophenyl)-1H-pyrazole-4-carboxylate

Produkt 1

HCID 13882127HCID 13882127, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A 5.5 g. portion of ethyl 5-cyano-1-(3-fluorophenyl)-4-pyrazolecarboxylate and 4.7 g. of potassium hydroxide were dissolved in 100 ml. of ethanol at the reflux temperature and the mixture was stirred at that temperature for2 hours. The mixture was then diluted to 350 ml. with cold water, and was heated slightly to obtain a solution which was made acid with concentratedhydrochloric acid. The product was precipitated by adding small amounts of ice, and the precipitated product was then collected by filtration and crystallized from ethanol-water to obtain 3.6 g. of the desired product, m.p. 215°-216°, having the following elemental analysis.

Aufarbeitung

  1. additionThe mixture was then diluted to 350 ml
  2. customto obtain a solution which
  3. customThe product was precipitated
  4. additionby adding small amounts of ice
  5. filtrationthe precipitated product was then collected by filtration
  6. customcrystallized from ethanol-water
  7. customto obtain 3.6 g

Quellen und Nachweise

ORD-Eintrag
ord-49179e162c62423e8ff31e70075bb35c
Quelldatensatz
uspto-grants-1988_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04775409

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