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

Iodine → (2R)-2,6-dimethylheptan-1-ol

HRID 28444
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 28444
[Mg].II.Br[CH2:5][CH2:6][CH:7]([CH3:9])[CH3:8].[Li+].[Cl-].Br[CH2:13][C@H:14]([CH3:17])[CH2:15][OH:16]>C1COCC1.[Cu](Cl)Cl>[CH3:17][C@H:14]([CH2:13][CH2:5][CH2:6][CH:7]([CH3:9])[CH3:8])[CH2:15][OH:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 807IodineHCID 78911-Bromo-3-methylbutane2×HCID 433294Lithium ChlorideHCID 5462224MagnesiumHCID 10441885(R)-(-)-3-Bromo-2-methyl-1-propanol

Produkt 1

HCID 10558744(2R)-2,6-dimethylheptan-1-ol

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24014Cupric ChlorideKatalysator
HCID 8028TetrahydrofuranLösungsmittel4×

Versuchsvorschrift

Magnesium turnings (2.04 g, 84 mmol) and a crystal of iodine were suspended in 5 mL THF for the addition of 1-bromo-3-methyl butane (0.3 mL, neat). The mixture was heated to start the Grignard formation. The remaining 1-bromo-3-methyl butane (8.63 mL, 72 mmol) was diluted in THF (60 mL) and added dropwise. The mixture was stirred at ambient temperature for 2 hours and cooled to −5° C. A solution of copper chloride (1.21 g, 9 mmol) and LiCl (0.76 g, 18 mmol) in THF (50 mL) was added dropwise keeping the temperature below 0° C. The resulting mixture was stirred for 20 min, and (R)-3-bromo-2-methylpropanol in THF (20 mL) was added dropwise while keeping the temperature below 0° C. The mixture was allowed to slowly reach ambient temperature overnight. The reaction mixture was quenched with ammonium hydroxide and water. The mixture was diluted with EtOAc and extracted with 3×20 mL EtOAc. The organics were washed with brine, dried (MgSO4), filtered and concentrated. The residual oil was purified via silica gel chromatography (90/10 Hexane/EtOAc) to give 2.67 g (R)-2,6-dimethyl heptan-1-ol.

Aufarbeitung

  1. temperatureThe mixture was heated
  2. additionadded dropwise
  3. temperaturecooled to −5° C
  4. customthe temperature below 0° C
  5. stirringThe resulting mixture was stirred for 20 min
  6. customthe temperature below 0° C
  7. customwas allowed to slowly reach ambient temperature overnight
  8. customThe reaction mixture was quenched with ammonium hydroxide and water
  9. additionThe mixture was diluted with EtOAc
  10. extractionextracted with 3×20 mL EtOAc
  11. washThe organics were washed with brine
  12. dry with materialdried (MgSO4)
  13. filtrationfiltered
  14. concentrationconcentrated
  15. customThe residual oil was purified via silica gel chromatography (90/10 Hexane/EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-c2d992af70f546238294c7b84d471bfd
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07419981B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion