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

Water → 5-Chloro-2-(4-fluorophenyl)-2-methoxyvaleric acid

HRID 599611
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 599611
[OH-].[Na+].[Cl:3][CH2:4][CH2:5][CH2:6][C:7]([C:14]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=1)([O:12][CH3:13])[C:8]([O:10]C)=[O:9].O>C1COCC1.CO>[Cl:3][CH2:4][CH2:5][CH2:6][C:7]([C:14]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=1)([O:12][CH3:13])[C:8]([OH:10])=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 962WaterHCID 14798Sodium Hydroxide2×HCID 67067459Methyl 5-chloro-2-(4-fluorophenyl)-2-methoxyvalerate

Produkt 1

HCID 670671515-Chloro-2-(4-fluorophenyl)-2-methoxyvaleric acidAusbeute 81,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittel2×
HCID 8028
Tetrahydrofuran
Lösungsmittel

Versuchsvorschrift

A 4 N sodium hydroxide solution (0.2 mL) was added to a mixed solution of methyl 5-chloro-2-(4-fluorophenyl)-2-methoxyvalerate (141 mg) in THF (1 mL) and methanol (0.5 mL), and the reaction solution was stirred at room temperature for 3.5 hours. Methanol (0.5 mL) and a 4 N sodium hydroxide solution (0.1 mL) were added to the reaction solution, and the reaction solution was further stirred at room temperature for 1.5 hours. Water was added to the reaction solution which was then washed with diethyl ether. 1 N hydrochloric acid (1.4 mL) and ethyl acetate were added to the resulting aqueous layer, and the organic layer was separated. The resulting ethyl acetate layer was washed with brine and dried over anhydrous magnesium sulfate. The resulting ethyl acetate layer was concentrated under reduced pressure to obtain 109 mg of the title compound. The property values of the compound are as follows.

Aufarbeitung

  1. stirringthe reaction solution was further stirred at room temperature for 1.5 hours
  2. washwas then washed with diethyl ether
  3. addition1 N hydrochloric acid (1.4 mL) and ethyl acetate were added to the resulting aqueous layer
  4. customthe organic layer was separated
  5. washThe resulting ethyl acetate layer was washed with brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationThe resulting ethyl acetate layer was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-4f264d2ed8b34311acace847a764ff30
Quelldatensatz
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07897632B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion