反応 #520154

ord-4966983d9fdf476783aaf4dd3fe37062

反応方程式

CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)O
z,z,z-6,9,12-Octadecatrienoic acid
OCCCO
propane-1,3-diol
O=[PH2]O
hypophosphorous acid
CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)OCCCOC(=O)CCCC/C=C\C/C=C\C/C=C\CCCCC
1,3-di-(z,z,z-6,9,12-octadecatrienoyloxy)propane

反応条件

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

後処理

  1. 1
    温度The mixture was cooled down to room temperature
  2. 2
    洗浄The resulting solution was washed with saturated sodium bicarbonate (3×70 mL) and saturated sodium chloride (3×70 mL)
  3. 3
    乾燥It was then dried over anhydrous sodium sulphate
  4. 4
    濃縮concentrated to dryness
  5. 5
    その他Residual mono-ester and fatty acid were removed by distillation in vacuo (180° C., 10−2 mbar)
  6. 6
    workup.DISSOLUTIONThe resulting oil was dissolved in petroleum ether
  7. 7
    その他Hexane was finally removed

実験手順

z,z,z-6,9,12-Octadecatrienoic acid (available from Sigma Chemicals) (0.180 mol, 50.0 g), propane-1,3-diol (0.086 mol, 6.5 g) and hypophosphorous acid (0.2 g) was heated with stirring to 160° C. under nitrogen. After 6 h, TLC (80:18:2 petroleum ether-ethyl ether-acetic acid) indicated that the reaction had gone to completion (Rf:0.56). The mixture was cooled down to room temperature and petroleum ether (700 mL) was added. The resulting solution was washed with saturated sodium bicarbonate (3×70 mL) and saturated sodium chloride (3×70 mL). It was then dried over anhydrous sodium sulphate and concentrated to dryness. Residual mono-ester and fatty acid were removed by distillation in vacuo (180° C., 10−2 mbar). The resulting oil was dissolved in petroleum ether to make up a 33% solution and was passed down a silica column. Hexane was finally removed to yield 1,3-di-(z,z,z-6,9,12-octadecatrienoyloxy)propane as a colourless oil.

出典

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