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Diethyl Ether → (2R)-1-(benzyloxy)pent-4-en-2-ol

HRID 217984
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 217984
[CH3:1][CH2:2]OCC.[CH2:6]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C@@H:7]1[O:9][CH2:8]1.C([Mg]Cl)=C.[Cl-].[NH4+]>C1COCC1.[Cu]I>[CH2:11]([O:10][CH2:6][C@H:7]([OH:9])[CH2:8][CH:1]=[CH2:2])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 3283Diethyl EtherHCID 25517Ammonium ChlorideHCID 159746(-)-Benzyl (R)-glycidyl etherHCID 178461836HCID 178461836, Verbindung

Produkt 1

HCID 10375318(2R)-1-(benzyloxy)pent-4-en-2-ol

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24350
Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
Katalysator
HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

Ether (100 ml) and copper(I) iodide (580 mg) were added to a solution of (R)-benzyl glycidyl ether (10.0 g) in THF (100 ml). The mixture was cooled to −78° C., and vinylmagnesium chloride (1.38 M, 53.0 ml) was added dropwise. The mixture was stirred overnight with gradual heating to room temperature. Ice was added to the reaction solution, and an ammonium chloride solution was further added. The aqueous layer was extracted with ethyl acetate, and the organic layer was washed with an ammonium chloride solution. The insoluble matter was removed by filtration through celite, and the solvent was evaporated under reduced pressure to obtain the title compound (12.5 g).

Aufarbeitung

  1. temperaturewith gradual heating to room temperature
  2. additionIce was added to the reaction solution
  3. extractionThe aqueous layer was extracted with ethyl acetate
  4. washthe organic layer was washed with an ammonium chloride solution
  5. customThe insoluble matter was removed by filtration through celite
  6. customthe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-66d8431238374018b9428ed53cb30a46
Quelldatensatz
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08198269B2

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