Reacción #8450

ord-338e450e2b7f4467853415ac44b79a17

Ecuación de reacción

CC(=O)c1ccc(O)cc1
p-hydroxyacetophenone
ClCCCBr
1-bromo-3-chloropropane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)c1ccc(OCCCCl)cc1
title compound
CC(=O)c1ccc(OCCCCl)cc1
p-chloropropoxyacetophenone

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux temperature for 18 hours
  2. 2
    Filtraciónfiltered
  3. 3
    ConcentraciónThe filtrate was concentrated in vacuo
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in ether
  5. 5
    Lavadowashed with water
  6. 6
    Secadodried over sodium sulfate
  7. 7
    Filtraciónfiltered
  8. 8
    Otroevaporated

Procedimiento

A mixture of p-hydroxyacetophenone (15 g) and 1-bromo-3-chloropropane (12 mL) in acetone (200 mL) was treated with potassium carbonate (17 g). The mixture was stirred at reflux temperature for 18 hours. The reaction was cooled to ambient temperature and filtered. The filtrate was concentrated in vacuo. The residue was dissolved in ether, washed with water, dried over sodium sulfate, filtered and evaporated to yield the title compound (23 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087757B2uspto-grants-2006_08