تفاعل #65822

ord-720c99001e6e47de9d4bb6669ec93d3a

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe mixture was removed from the cold bath for 30 min
  2. 2
    ترشيحfiltered through celite
  3. 3
    غسيلwashing with 75 ml ether
  4. 4
    غسيلThe filtrate was washed with 2×100 ml H2O and with 50 ml 10% NaHCO3
  5. 5
    تجفيفThe ether was dried over MgSO4
  6. 6
    أخرىremoved by rotary evaporation

الإجراء التجريبي

To a rapidly-stirred slurry of 1.29 g (4.99 mmol) methyl (R)-3-hydroxytetradecanoate and 0.45 ml (5.2 mmol) bromoacetyl bromide in 25 ml hexanes at 0° C. in a flame-dried flask under N2 was added 0.42 ml (5.2 mmol)pyridine all at once. The mixture was removed from the cold bath for 30 min. The mixture was suction filtered through celite, washing with 75 ml ether. The filtrate was washed with 2×100 ml H2O and with 50 ml 10% NaHCO3. The ether was dried over MgSO4 and removed by rotary evaporation, giving 1.70 g (90%) crude (R)-3-[(bromoacetyl)oxy]tetradecanoic acid methyl ester as a yellow oil. Analytically pure samples could be prepared by subjecting the oil to radial chromatography, eluting with CH2Cl2.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05420305uspto-grants-1995_05