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Hydrogen Peroxide → (R)-2-Hydroxymethyl-4-methylpentanoic acid

HRID 907201
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 907201
C([C@H]1COC(=O)N1[C:14](=[O:22])[C@@H:15]([CH2:20][OH:21])[CH2:16][CH:17]([CH3:19])[CH3:18])C1C=CC=CC=1.C1C[O:26]CC1.OO.O.[OH-].[Li+].[OH-].[K+].S([O-])([O-])=O.[Na+].[Na+]>O.C(Cl)(Cl)Cl>[OH:21][CH2:20][C@@H:15]([CH2:16][CH:17]([CH3:18])[CH3:19])[C:14]([OH:22])=[O:26]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 6

HCID 784Hydrogen PeroxideHCID 8028TetrahydrofuranHCID 14797Potassium HydroxideHCID 24437Sodium SulfiteHCID 168937Lithium hydroxide, monohydrateHCID 59556783(S)-4-Benzyl-3-((R)-2-hydroxymethyl-4-methylpentanoyl)oxazolidin-2-one

Produkt 1

HCID 13017555
(R)-2-Hydroxymethyl-4-methylpentanoic acid
Ausbeute 90,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel3×HCID 6212ChloroformLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Intermediate (2b) (13.9 g, 40.8 mmol) was dissolved in THF (200 mL, 2 mol) and stirred at 0° C. 9 M hydrogen peroxide in water (46.3 mL) was added, followed by dropwise addition of 1.5 M lithium hydroxide monohydrate in water (54.4 mL). The mixture was then warmed to room temperature and stirred for 2.5 hours. Potassium hydroxide (4.6 g, 81.6 mmol) was added and the mixture was heated at 60° C. for 30 minutes and then cooled at room temperature. To this was added a solution of sodium sulfite (10 g in 200 mL water) followed by water and chloroform (200 mL of each). The aqueous layer was extracted twice more with CHCl3 (150 mL), acidified and extracted with EtOAc. The organic layer was then washed with saturated aqueous NaCl, dried over MgSO4, filtered, and rotovaped to provide intermediate (2c) (5.4 g).

Aufarbeitung

  1. temperatureThe mixture was then warmed to room temperature
  2. stirringstirred for 2.5 hours
  3. temperaturethe mixture was heated at 60° C. for 30 minutes
  4. temperaturecooled at room temperature
  5. extractionThe aqueous layer was extracted twice more with CHCl3 (150 mL)
  6. extractionextracted with EtOAc
  7. washThe organic layer was then washed with saturated aqueous NaCl
  8. dry with materialdried over MgSO4
  9. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-32f742c8cd5742a48aa168d12138d615
Quelldatensatz
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08013005B2

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