反应 #417899

ord-c247f44ca28e4ae882317b74efb8bdc6

反应方程式

OCCO
ethylene glycol
CC(C)(C)c1cc(O)cc(C(C)(C)C)c1O
3,5-Di-tert-butylhydroquinone
BrCCBr
1,2-dibromoethane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)(C)c1cc2c(c(C(C)(C)C)c1)OC=CO2
title compound
CC(C)(C)c1cc2c(c(C(C)(C)C)c1)OC=CO2
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. 1
    其他to quench
  2. 2
    其他the reaction
  3. 3
    萃取the organic compound was extracted by CH2Cl2
  4. 4
    浓缩The resulting solution was concentrated
  5. 5
    其他to afford a crude oil
  6. 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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08877390B2uspto-grants-2014_11