反応 #520156

ord-509117f4412d48a78b57464e78a9390b

反応方程式

CCCCCCCC/C=C\CCCCCCCCCCCCCC(=O)OCCCO
1-hydroxy-3-(z-15-tetracosenoyloxy)propane
CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)O
z,z,z-6,9,12-octadecatrienoic acid
O=[PH2]O
hypophosphorous acid
CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)OCCCOC(=O)CCCCCCCCCCCCC/C=C\CCCCCCCC
1-(z,z,z-6,9,12-octadecatrienoyloxy)-3-(z-15-tetracosenoyloxy)propane

反応条件

温度
160°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他prepared
  2. 2
    温度was heated
  3. 3
    その他had reacted (Rf: 0.60)
  4. 4
    温度The mixture was cooled down to room temperature
  5. 5
    洗浄The resulting solution was washed with saturated sodium bicarbonate (3×80 mL) and saturated sodium chloride (3×80 mL)
  6. 6
    乾燥It was then dried over anhydrous sodium sulphate
  7. 7
    濃縮concentrated
  8. 8
    その他purified by flash chromatography on silica gel (19:1 petroleum ether-ethyl ether)

実験手順

A mixture of 1-hydroxy-3-(z-15-tetracosenoyloxy)propane, prepared according to Description 3, (0.045 mol, 19.0 g), z,z,z-6,9,12-octadecatrienoic acid (0.054 mol, 15.0 g) and hypophosphorous acid (0.4 g) was heated with stirring to 160° C. under nitrogen. After 5 h, TLC (80:18:2 petroleum ether-ethyl ether-acetic acid) indicated that most of the mono-ester had reacted (Rf: 0.60). The mixture was cooled down to room temperature and petroleum ether (800 mL) was added. The resulting solution was washed with saturated sodium bicarbonate (3×80 mL) and saturated sodium chloride (3×80 mL). It was then dried over anhydrous sodium sulphate, concentrated and purified by flash chromatography on silica gel (19:1 petroleum ether-ethyl ether) to yield 1-(z,z,z-6,9,12-octadecatrienoyloxy)-3-(z-15-tetracosenoyloxy)propane as a pale yellow oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06664406B1uspto-grants-2003_12