반응 #50778

ord-68e95a88262e42688a7ba4b9a9a83427

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도is refluxed for 4 hours
  2. 2
    농축The reaction mixture is then concentrated on a vacuum rotary evaporator
  3. 3
    기타the residue is recrystallized from methanol

실험 절차

A suspension of 11.4 g (30 mmol) of 5,7-di-tert-butyl-3-[4-(2-hydroxyethoxy)phenyl]ben-zofuran-2-one (compound (105), Example 3) and 9.4 g (31 mmol) of stearoyl chloride in 60 ml of toluene is refluxed for 4 hours. The reaction mixture is then concentrated on a vacuum rotary evaporator, and the residue is recrystallized from methanol to give 17.3 g (89%) of 5,7-di-tert-butyl-3-[4-(2-stearoyloxyethoxy)phenyl]benzofuran-2-one, m.p. 54°-60° C. (compound (107), Table 1).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05428162uspto-grants-1995_06