반응 #482432

ord-36989a97950047ca804b9329f2cd9f52

반응 방정식

Cc1ccc(O)c(O)c1
4-methylcatechol
BrCCBr
1,2-dibromoethane
O=C([O-])[O-].[K+].[K+]
K2CO3
Cc1ccc2c(c1)OCCO2
title intermediate
수율 50.0%
Cc1ccc2c(c1)OCCO2
6-Methyl-1,4-benzodioxane
수율 50.0%

반응 조건

온도
130°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to cool to ambient temperature
  2. 2
    여과After the mixture was filtered through celite
  3. 3
    workup.ADDITIONthe solution was diluted with brine (800 mL)
  4. 4
    추출extracted with organic solvents (CH2Cl2/hexane/EtOAc: 1:3:1,3×500 mL)
  5. 5
    건조The organic layer was dried over Na2SO4
  6. 6
    여과filtered
  7. 7
    농축concentrated
  8. 8
    기타to provide a crude oil
  9. 9
    세척Flash silica gel chromatography eluting with hexane (100%) gradient to ether/hexane (8:2)

실험 절차

A mixture of 4-methylcatechol (33.04 g, 266.1 mmol), 1,2-dibromoethane (100 g, 532.3 mmol), K2CO3 (75.4 g, 545.5 mmol) and sodium iodide (0.2 g, 1.33 mmol) in ethylene glycol (500 mL) was heated to 130° C. under nitrogen for five hours. The solution was allowed to cool to ambient temperature and stirred overnight. After the mixture was filtered through celite, the solution was diluted with brine (800 mL) and extracted with organic solvents (CH2Cl2/hexane/EtOAc: 1:3:1,3×500 mL). The organic layer was dried over Na2SO4, filtered and concentrated to provide a crude oil. Flash silica gel chromatography eluting with hexane (100%) gradient to ether/hexane (8:2) afforded the title intermediate as a colorless oil 20.0 g (50%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06605596B2uspto-grants-2003_08