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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2117682Erstellt: 25. Oktober 2026

Diethyl Ether → 1-Bromo-7-(prop-2-yn-1-yloxy)heptane

https://huagongshe.com/reaction/2117682

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktPropargyl alcoholHCID 7859—
EduktSodium HydroxideHCID 14798—
Edukt1,7-DibromoheptaneHCID 78309—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
Produkt1-Bromo-7-(prop-2-yn-1-yloxy)heptaneHCID 2189554017%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

25% (w/w) aq. NaOH (700 ml) was added to a stirred mixture of propargyl alcohol (70 g), tetra-butyl ammonium bromide (3.5 g) and 1,7-dibromoheptane (322 g) maintaining the temperature below 30° C. The reaction mixture was heated at 60° C. for 5 hrs then allowed to cool to room temperature and stirred overnight. Diethyl ether (350 ml) and water (280 ml) were added, the mixture stirred and allowed to settle. The aqueous layer was extracted with diethyl ether (210 ml), the organic layers combined, dried (MgSO4). The solution was concentrated to give 280 g of crude material. 140 g Of the crude was purified by chromatography on Biotage (800 g) eluting with petroleum ether then petroleum ether:ethyl acetate (100:1 followed by 100:1.5) to give the title compound (49.6 g). NMR—300 MHz—δ (CDCl3)—4.05 (2H, d, J 2 Hz), 3.45 (2H, t, J 6.5 Hz), 3.35 (2H, t, J 7 Hz), 2.35 (1H, s), 1.8 (2H, m), 1.5 (2H, m), 1.3 (4H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07442719B2
Quelldatensatzuspto-grants-2008_10
ORD IDord-928972620f544a12a2876e271dcbf73e
Quellennotizuspto-grants-2008_10