反应 #417899
ord-c247f44ca28e4ae882317b74efb8bdc6
反应方程式
ethylene glycol
3,5-Di-tert-butylhydroquinone
1,2-dibromoethane
potassium carbonate
→
title compound
5,7-di-tert-butyl-1,4-benzodioxin
溶剂
反应条件
温度
120°CELSIUS
详细条件
See reaction.notes.procedure_details.
后处理
- 1其他to quench
- 2其他the reaction
- 3萃取the organic compound was extracted by CH2Cl2
- 4浓缩The resulting solution was concentrated
- 5其他to afford a crude oil
- 6其他The crude oil was then chromatographed (silica, hexane/ethyl acetate=20:1) mixture
实验过程
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).