반응 #46732

ord-608f69a0b7be4c06a95c0fdcf4ccd517

반응 방정식

CC(=O)c1ccc(O)cc1O
2,4-dihydroxy actophenone
CCCCCCCCBr
1-bromooctane
CCCCCCCCOc1ccc(C(C)=O)c(O)c1
1-(2-Hydroxy-4-octyloxy-phenyl)-ethanone

용매

반응 조건

온도
55°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONpoured onto H2O (100 mL)
  2. 2
    추출the aqueous phase extracted with diethyl ether (3×)
  3. 3
    건조The combined organic fractions was dried (MgSO4)
  4. 4
    여과filtered
  5. 5
    기타evaporated to dryness
  6. 6
    기타purified by column chromatography (SiO2; EtOAc/PE80-100° C.=1:10)
  7. 7
    기타to yield 4.39 g (66%) as yellow oil

실험 절차

A slurry of 2,4-dihydroxy actophenone (3.8 g; 25 mmol) and KHCO3 (2.75 g; 27.5 mmol) in DMF (50 mL) was stirred at 50° C. for 1 hour and then added 1-bromooctane (4.75 mL; 27.5 mmol). The reaction mixture was stirred at 50-60° C. for 7 days, poured onto H2O (100 mL) and the aqueous phase extracted with diethyl ether (3×). The combined organic fractions was dried (MgSO4), filtered, evaporated to dryness and purified by column chromatography (SiO2; EtOAc/PE80-100° C.=1:10) to yield 4.39 g (66%) as yellow oil. MS (direct; Cl): 265 (MH+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741352B2uspto-grants-2010_06