反応 #1552098

ord-8a52d0998624438298eccce1694258fb

反応方程式

CCCCCCCCCCCCCCCCOCC(O)CO
1-hexadecyl-glycerol
ClC(c1ccccc1)(c1ccccc1)c1ccccc1
triphenylchloromethane
C1CCOC1
tetrahydrofuran
CC#N
acetonitrile
CCCCCCCCCCCCCCCCOC[C@@H](O)COC(c1ccccc1)(c1ccccc1)c1ccccc1
1-hexadecyl-3-trityl-sn-glycerol

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度the reaction mixture was refluxed for 17 hours
  2. 2
    workup.ADDITIONpoured on ice (1 kilogram)
  3. 3
    抽出extracted thrice with 250 ml diethyl ether
  4. 4
    洗浄The organic phase was washed consecutively with 100 ml water, 100 ml
  5. 5
    workup.ADDITIONdilute (1.5%) sulfuric acid, 100 ml water, 100 ml concentrated aqueous sodium bicarbonate
  6. 6
    乾燥The obtained organic phase was dried over anhydrous sodium sulfate
  7. 7
    その他the solvent was thereafter removed under reduced pressure
  8. 8
    workup.DISSOLUTIONThe residue was dissolved in 200 ml ethyl acetate
  9. 9
    温度the resulting solution was cooled at −20° C. overnight
  10. 10
    その他was then centrifuged at −5° C.
  11. 11
    workup.ADDITIONthe mother liquid solution was poured off
  12. 12
    workup.DISSOLUTIONThe solid was dissolved in hexane and refrigerated overnight at 5° C
  13. 13
    ろ過Filtration of the precipitate

実験手順

40 grams of 1-hexadecyl-glycerol and 43 grams triphenylchloromethane were added to a mixture of 500 ml dry tetrahydrofuran and 130 ml dry acetonitrile. 35 ml of dry triethylamine was added, and the reaction mixture was refluxed for 17 hours. The reaction mixture was then cooled to room temperature, poured on ice (1 kilogram) and extracted thrice with 250 ml diethyl ether. The organic phase was washed consecutively with 100 ml water, 100 ml dilute (1.5%) sulfuric acid, 100 ml water, 100 ml concentrated aqueous sodium bicarbonate and again with 100 ml water. The obtained organic phase was dried over anhydrous sodium sulfate and the solvent was thereafter removed under reduced pressure. The residue was dissolved in 200 ml ethyl acetate and the resulting solution was cooled at −20° C. overnight. The mixture was then centrifuged at −5° C. and the mother liquid solution was poured off. The solid was dissolved in hexane and refrigerated overnight at 5° C. Filtration of the precipitate yielded pure 1-hexadecyl-3-trityl-sn-glycerol.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08999960B2uspto-grants-2015_04