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Methanol → (1-Propylcyclobutyl)methanol

HRID 9231
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 9231
[Li+].[BH4-].CO.C[O:6][C:7]([C:9]1([CH2:13][CH2:14][CH3:15])[CH2:12][CH2:11][CH2:10]1)=O.[OH-].[Na+]>CCOCC>[CH2:13]([C:9]1([CH2:7][OH:6])[CH2:12][CH2:11][CH2:10]1)[CH2:14][CH3:15]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 887MethanolHCID 14798Sodium HydroxideHCID 4148881Lithium borohydrideHCID 693808831-Propyl-cyclobutanecarboxylic acid methyl ester

Produkt 1

HCID 21985998(1-Propylcyclobutyl)methanolAusbeute 87 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283
Diethyl Ether
Lösungsmittel

Versuchsvorschrift

LiBH4 (524 mg, 24 mmol) and methanol (1 mL) were added to a 0° C. solution of 1-2 (1.935 g, 11.4 mmol) in ether (22 mL). After 1 h at 0° C. and 1.5 h at room temperature, 41 mL 2 M NaOH was slowly added and the resulting mixture was stirred for 1 h. The mixture was then extracted with dichloromethane (3×40 mL) and the combined dichloromethane solution was washed with saturated NH4Cl solution and brine (150 mL each). The organic solution was then dried (Na2SO4), filtered and evaporated. Purification by flash chromatography on silica gel (dichloromethane) gave 1-3 (1.229 g, 87%).

Aufarbeitung

  1. extractionThe mixture was then extracted with dichloromethane (3×40 mL)
  2. washthe combined dichloromethane solution was washed with saturated NH4Cl solution and brine (150 mL each)
  3. dry with materialThe organic solution was then dried (Na2SO4)
  4. filtrationfiltered
  5. customevaporated
  6. customPurification by flash chromatography on silica gel (dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-081cc9df8950478ca48b57a906302cc0
Quelldatensatz
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07091231B2

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