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

Hydrogen Peroxide → 2-Allyloctanoic acid

HRID 1180701
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1180701
OO.O.[OH-].[Li+].C(OC(N([C@@H](C1C=CC=C(OC)C=1)C)[C:12](=[O:23])[CH:13]([CH2:20][CH:21]=[CH2:22])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=O)C.S([O-])([O-])=[O:35].[Na+].[Na+]>C1COCC1.O>[CH2:20]([CH:13]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[C:12]([OH:23])=[O:35])[CH:21]=[CH2:22]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 784Hydrogen PeroxideHCID 24437Sodium SulfiteHCID 168937Lithium hydroxide, monohydrateHCID 69502062N-Ethyloxycarbonyl-N-(2-allyloctanoyl)-(R)-1-(3-methoxyphenyl)ethylamine

Produkt 1

HCID 108451992-Allyloctanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
2×
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

An aqueous solution of hydrogen peroxide (31% by weight; 0.5 ml, 55.0 mmol) and 0.043 g (1.0 mmol) of lithium hydroxide monohydrate were added dropwise to a solution of 0.20 g (0.50 mmol) of N-ethyloxycarbonyl-N-(2-allyloctanoyl)-(R)-1-(3-methoxyphenyl)ethylamine ((1R,2S):(1R,2R)=77:23) in a mixture of 4 ml of THF and 1 ml of water on an ice bath. The mixture was stirred on an ice bath for 3 hours and then at room temperature for 20 hours. A 2 N aqueous solution of sodium sulfite (5 ml) was added dropwise to the reaction mixture on an ice bath, and the resulting mixture was stirred at room temperature for 2 hours. Water (15 ml) was added to the reaction mixture, and the whole mixture was washed with 5 ml of ethyl acetate. To the aqueous layer was added 2 ml of a 1 N aqueous solution of hydrochloric acid (pH=2), and the resulting mixture was extracted with two 40-ml portions of ethyl acetate. The organic layer was concentrated under reduced pressure to give 0.078 g (83%, 62% ee) of the title compound as a colorless oil.

Aufarbeitung

  1. waitat room temperature for 20 hours
  2. stirringthe resulting mixture was stirred at room temperature for 2 hours
  3. washthe whole mixture was washed with 5 ml of ethyl acetate
  4. additionTo the aqueous layer was added 2 ml of a 1 N aqueous solution of hydrochloric acid (pH=2)
  5. extractionthe resulting mixture was extracted with two 40-ml portions of ethyl acetate
  6. concentrationThe organic layer was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-a4b4b5d7cc334bbfb66cb28f27c28bd9
Quelldatensatz
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07282605B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion