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Diethyl Ether → 3,3-Difluoro-4-methylpentane-1,4-diol

HRID 745636
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 745636
[CH3:1][Li].[F:3][C:4]([F:13])([CH2:10][CH2:11][OH:12])C(OCC)=O.CC[O:16][CH2:17][CH3:18]>>[CH3:1][C:17]([OH:16])([CH3:18])[C:4]([F:13])([F:3])[CH2:10][CH2:11][OH:12]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 3283Diethyl EtherHCID 13189245Ethyl 2,2-difluoro-4-hydroxybutanoateHCID 178418348HCID 178418348, Verbindung

Produkt 1

HCID 131892463,3-Difluoro-4-methylpentane-1,4-diol

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

To a solution of 311 mL of 1.6M ethereal methyllithium (0.498 mol) of 0° was added dropwise 11.16 g (0.066 mol) of ethyl 2,2-difluoro-4-hydroxybutanoate in 150 mL of ether. The mixture was stirred at 0° C. for 1 hr and at 25° C. for 17 hr. The mixture was quenched by adding 14 mL of saturated brine at 0° C. The mixture was poured into saturated brine and the product was isolated with ether. The ether layers were dried over anhydrous magnesium sulfate, filtered, and evaporated to dryness. The residue was chromatographed on 0.06-0.20 mm of silica gel to give 4-methyl-3,3-difluoro-1,4-pentanediol.

Aufarbeitung

  1. customThe mixture was quenched
  2. additionby adding 14 mL of saturated brine at 0° C
  3. additionThe mixture was poured into saturated brine
  4. customthe product was isolated with ether
  5. dry with materialThe ether layers were dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customevaporated to dryness
  8. customThe residue was chromatographed on 0.06-0.20 mm of silica gel

Quellen und Nachweise

ORD-Eintrag
ord-8480cec98dc64fe2ae1e34f4a09358a3
Quelldatensatz
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04599330

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