반응 #1470440

ord-e22b4b8e6d694a8ebfecbf2afe969cc3

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to reach room temperature
  2. 2
    workup.STIRRINGthe two-phase mixture was stirred for 1 hr
  3. 3
    세척The organic phase was washed with 3% aqueous HCl
  4. 4
    기타dried
  5. 5
    기타Solvents were removed under vacuum
  6. 6
    workup.ADDITIONThe fractions containing the ester
  7. 7
    기타evaporated under vacuum

실험 절차

Synthesis of propofol hemiadipate Triethylamine (6.26 ml, 45 mmol) and 4-dimethylaminopyridine (50 mg, 0.4 mmol) in methylene chloride (30 ml) were added to a solution of 2,6-diisopropylphenol (5.2 ml, 28 mmol) and adipoyl chloride (4.4 ml, 30 mmol) in methylene chloride (50) at 0° C. The mixture was allowed to reach room temperature and stirred at that temperature for 2 hr. Water (50 ml) was added, and the two-phase mixture was stirred for 1 hr. The organic phase was washed with 3% aqueous HCl and then dried. Solvents were removed under vacuum, and the oily residue was chromatogrammed on a silica gel column using chloroform-methanol (10:0.1) and then chloroform-methanol-acetic acid (10:0.1:0.01). The fractions containing the ester were pooled and evaporated under vacuum to yield 3.4 g (40% yield) of 2,6-diisopropylphenol hydrogen adipate (propofol hemiadipate) as an oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06254853B1uspto-grants-2001_07