Reaktion #417899
ord-c247f44ca28e4ae882317b74efb8bdc6
Reaktionsgleichung
ethylene glycol
3,5-Di-tert-butylhydroquinone
1,2-dibromoethane
potassium carbonate
→
title compound
5,7-di-tert-butyl-1,4-benzodioxin
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
120°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeto quench
- 2Sonstigethe reaction
- 3Extraktionthe organic compound was extracted by CH2Cl2
- 4EinengenThe resulting solution was concentrated
- 5Sonstigeto afford a crude oil
- 6SonstigeThe crude oil was then chromatographed (silica, hexane/ethyl acetate=20:1) mixture
Vorschrift
3,5-Di-tert-butylhydroquinone (3.33 g, 15 mmol) was combined with 1,2-dibromoethane (5.6 g), potassium carbonate (4.35 g) and ethylene glycol (25 mL). The mixture was heated in a 120° C. oil bath under an Ar atmosphere for 12 h. Water was added to the reaction mixture to quench the reaction and then the organic compound was extracted by CH2Cl2. The resulting solution was concentrated to afford a crude oil. The crude oil was then chromatographed (silica, hexane/ethyl acetate=20:1) mixture to afford the title compound (Rf=0.5, 5:1 hexane/ethyl acetate). 1H NMR (500 MHz, CDCl3): δ 7.03 (d, J=2 Hz, 1H), 6.93 (d, J=2 Hz, 1H), 4.34 (s, 4H), 1.53 (s, 9H), 1.43 (s, 9H).