反応 #1470440

ord-e22b4b8e6d694a8ebfecbf2afe969cc3

反応方程式

O
Water
CC(C)c1cccc(C(C)C)c1O
propofol
CC(C)c1cccc(C(C)C)c1O
2,6-diisopropylphenol
O=C(Cl)CCCCC(=O)Cl
adipoyl chloride
CC(C)c1cccc(C(C)C)c1OC(=O)CCCCC(=O)O
2,6-diisopropylphenol hydrogen adipate
収率 40.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他to reach room temperature
  2. 2
    workup.STIRRINGthe two-phase mixture was stirred for 1 hr
  3. 3
    洗浄The organic phase was washed with 3% aqueous HCl
  4. 4
    その他dried
  5. 5
    その他Solvents were removed under vacuum
  6. 6
    workup.ADDITIONThe fractions containing the ester
  7. 7
    その他evaporated under vacuum

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06254853B1uspto-grants-2001_07