Diethyl Ether → 4,5-Epoxy-4-(4'-fluorophenyl)-1-pentyne

HRID 414641

Reaktionsgleichung

Reaktionsgleichung von HRID 414641
[CH2:1]([Mg]Br)[C:2]#C.Cl[CH2:7][C:8]([C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=1)=[O:9].[CH2:17](OCC)C>>[O:9]1[CH2:17][C:8]1([C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=1)[CH2:7][C:1]#[CH:2]

Komponenten

4

Edukt 3

HCID 3283Diethyl Ether2×HCID 1202482-Chloro-4'-fluoroacetophenoneHCID 178455849HCID 178455849, Verbindung

Produkt 1

HCID 144246744,5-Epoxy-4-(4'-fluorophenyl)-1-pentyneAusbeute 79 %

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

To a solution of 23.1 g (0.16 mol) of propargylmagnesium bromide (J. Am. Chem. Soc., 83, 1686, 1961) in 50 mL of dry diethyl ether at 25° C. was added 20.0 g (0.115 mol) of 2-chloro-4'-fluoroacetophenone in 150 mL of diethyl ether over a 0.25 hour period. The solution was stirred at 25° C. for 15 hours and then quenched with 50 mL of saturated NH4Cl. The layers were separated and the aqueous phase extracted twice with 100 mL diethyl ether. The combined ether extracts were dried (MgSO4) and the solvent removed at reduced pressure. This residue was dissolved in 250 mL of dry diethyl ether and added to 4.9 g of pulverized NaOH. This mixture was stirred at 24° C. for 3.5 hours and then 0.5 g of NaOH was added. After an additional 2.5 hours, the mixture was poured into 100 mL of H2O and extracted with diethyl ether. The ether layer was separated, dried (MgSO4) and concentrated under reduced pressure. Distillation under reduced pressure (94°-95° C. at 0.65 mmHg) yielded 16 g (79%) of 4,5-epoxy-4-(4'-fluorophenyl)-1-pentyne as an oil, homogeneous by TLC and spectroscopic criteria; Rf 0.75 (1:1 hexanes-diethyl ether): IR (film) 3290, 1600, 1505, 1225 cm-1 ; 1HNMR (300 MHz, CDCl3) δ 7.5-7.4 (m, 2H), 7.1-7.05 (m, 2H, 3.02 (ABq, 2H, JAB =6.0 Hz, ΔνAB =119.8 Hz), 2.92 (t, 2H, J=2 Hz), 2.07 (t, 1H, J=2 Hz).

Aufarbeitung

  1. customquenched with 50 mL of saturated NH4Cl
  2. customThe layers were separated
  3. extractionthe aqueous phase extracted twice with 100 mL diethyl ether
  4. dry with materialThe combined ether extracts were dried (MgSO4)
  5. customthe solvent removed at reduced pressure
  6. dissolutionThis residue was dissolved in 250 mL of dry diethyl ether
  7. additionadded to 4.9 g of pulverized NaOH
  8. stirringThis mixture was stirred at 24° C. for 3.5 hours
  9. addition0.5 g of NaOH was added
  10. waitAfter an additional 2.5 hours
  11. additionthe mixture was poured into 100 mL of H2O
  12. extractionextracted with diethyl ether
  13. customThe ether layer was separated
  14. dry with materialdried (MgSO4)
  15. concentrationconcentrated under reduced pressure
  16. distillationDistillation under reduced pressure (94°-95° C. at 0.65 mmHg)

Quellen und Nachweise

ORD-Eintrag
ord-d26fb6abd246428bb3334229f041105e
Quelldatensatz
uspto-grants-1988_12
Patentnummer
US04792614

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