반응 #1447098

ord-eeed7cb84df54cc28056c5c5beb05544

반응 방정식

Cl
hydrochloric acid
CCc1ccc(Cc2cc(Br)c(OC)cc2NC(C)=O)cc1
N-[4-bromo-2-(4-ethyl-benzyl)-5-methoxy-phenyl]-acetamide
CCc1ccc(Cc2cc(Br)c(OC)cc2N)cc1
title compound
CCc1ccc(Cc2cc(Br)c(OC)cc2N)cc1
4-Bromo-2-(4-ethyl-benzyl)-5-methoxy-phenylamine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The solution is heated
  2. 2
    온도at reflux temperature for 8 h
  3. 3
    농축concentrated under reduced pressure
  4. 4
    기타to remove most of the alcohol
  5. 5
    workup.ADDITIONAqueous NaHCO3 solution is added to the rest
  6. 6
    추출the resulting mixture is extracted twice with ethyl acetate
  7. 7
    세척The combined organic extracts are washed with brine
  8. 8
    건조dried (Na2SO4)
  9. 9
    농축concentrated

실험 절차

Half-concentrated hydrochloric acid (5 mL) is added to a solution of N-[4-bromo-2-(4-ethyl-benzyl)-5-methoxy-phenyl]-acetamide (2.8 g) in isopropanol (20 mL). The solution is heated at reflux temperature for 8 h and then concentrated under reduced pressure to remove most of the alcohol. Aqueous NaHCO3 solution is added to the rest and the resulting mixture is extracted twice with ethyl acetate. The combined organic extracts are washed with brine, dried (Na2SO4) and concentrated to give the title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07879806B2uspto-grants-2011_02