تفاعل #324363

ord-fd2c285cb6f84ea697e1388fb53f2459

معادلة التفاعل

CN(C)CC(O)CO
3-(dimethylamino)-1,2-propanediol
CCN=C=NCCCN(C)C
EDCI
CCOC(C)=O
EtOAc
CCCCC/C=C\C/C=C\CCCCCCCC(=O)O
linoleic acid
CCCCCC=CCC=CCCCCCCCC(=O)OCC(CN(C)C)OC(=O)CCCCCCCC=CCC=CCCCCC
ester
CCCCCC=CCC=CCCCCCCCC(=O)OCC(CN(C)C)OC(=O)CCCCCCCC=CCC=CCCCCC
Octadeca-9,12-dienoic acid 3-dimethylamino-2-octadeca-9,12-dienoyloxy-propyl ester

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred at room temperature overnight
  2. 2
    أخرىthe completion of the reaction
  3. 3
    استخلاصextracted with ethyl acetate (2×100 mL)
  4. 4
    غسيلThe combined organic layers were washed with water (100 mL), saturated NaHCO3 (100 mL)
  5. 5
    تجفيفdried over Na2SO4
  6. 6
    أخرىConcentration of the organic layer provided the crude product which
  7. 7
    أخرىwas purified by column chromatography (silica gel, eluent: 20% EtOAc in hexanes)
  8. 8
    workup.ADDITIONThe fractions containing pure product
  9. 9
    تركيزconcentrated

الإجراء التجريبي

To a solution of the linoleic acid (25 g, 89.1 mmol) in anhydrous DMF (60 mL), diisopropyl ethylamine (17 mL, 100 mml) was added at room temperature with stirring followed by 3-(dimethylamino)-1,2-propanediol (4.8 g, 40.5 mmol) and EDCI (17.25 g, 89.9 mmol) and the mixture was stirred at room temperature overnight. The TLC of the reaction mixture (eluent 20% EtOAc in hexanes) showed the completion of the reaction. The reaction mixture was poured into ice water and extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with water (100 mL), saturated NaHCO3 (100 mL) and dried over Na2SO4. Concentration of the organic layer provided the crude product which was purified by column chromatography (silica gel, eluent: 20% EtOAc in hexanes). The fractions containing pure product was pooled and concentrated. The pure ester was isolated as a clear liquid (5.7 g, 22%). MS m/z 645 (M+H). 1H NMR CDCl3 δ 0.88 (t, J=6.3 Hz, 6H), 1.20-1.39 (m, 28H), 1.61 (t, J=4.9 Hz, 12H), 2.03-2.08 (m, 8H), 2.26-2.38 (m, 10H), 2.44-2.56 (m, 2H), 2.76 (t, J=6.3 Hz, 4H), 4.09 (dd, J=6.1 Hz & 11.9 Hz, 1H), 4.36 (dd, J=3.3 & 11.9 Hz, 1H), 5.29-5.34 (m, 1H), 5.34-5.41 (m, 8H). 13C NMR CDCl3 δ 14.30, 22.79, 25.08, 25.10, 25.83, 27.40, 29.26, 29.30, 29.34, 29.42, 29.55, 29.83, 31.73, 34.32, 34.58, 46.01, 59.37, 64.02, 128.08, 128.24, 130.21, 130.42, 173.39, 173.65.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08642076B2uspto-grants-2014_02