StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Lithium Hydroxide → 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid

HRID 12877
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 12877
C([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([C:17]([CH3:20])([CH3:19])[CH3:18])[C:10]=1[C:11]1[CH:15]=[C:14]([Cl:16])[O:13][N:12]=1)=[O:5])C.[OH-].[Li+]>C(O)C>[C:17]([N:9]1[C:10]([C:11]2[CH:15]=[C:14]([Cl:16])[O:13][N:12]=2)=[C:6]([C:4]([OH:5])=[O:3])[CH:7]=[N:8]1)([CH3:20])([CH3:18])[CH3:19]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 3939Lithium HydroxideHCID 670210411-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid ethyl ester

Produkt 1

HCID 670209951-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acidAusbeute 79,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

A solution of 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (55.3 mg, 0.18 mmol) in absolute ethanol (0.93 mL, 0.2M) was treated with a 2M aqueous lithium hydroxide solution (0.18 mL, 0.37 mmol). The reaction was stirred at 25° C. for 1.5 h and then was heated to 100° C. for 1 h. At this time, the reaction was allowed to cool to 25° C. and was stirred at 25° C. overnight. At this time, the reaction was concentrated in vacuo. The residue was treated with water followed by acidification to pH=1 with a 1N aqueous hydrochloric acid solution. The resulting precipitate that formed was collected by filtration, washed with water and hexanes and dried in vacuo to afford 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid (38.7 mg, 77%) as an off-white solid.

Aufarbeitung

  1. temperaturewas heated to 100° C. for 1 h
  2. temperatureto cool to 25° C.
  3. stirringwas stirred at 25° C. overnight
  4. concentrationAt this time, the reaction was concentrated in vacuo
  5. additionThe residue was treated with water
  6. customThe resulting precipitate that formed
  7. filtrationwas collected by filtration
  8. washwashed with water and hexanes
  9. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-91730036d6fa4ebeb4f0f77293c28356
Quelldatensatz
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07728029B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion