Sodium hydride → 2-Methyl-alpha-[[4-(tetradecyloxy)phenyl]methyl]-1,3-dioxolane-2-propanoic acid, ethyl ester

HRID 235703

Reaktionsgleichung

Reaktionsgleichung von HRID 235703
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[CH:5][CH:4]=1.[CH2:24]1[O:36][C:27]([CH3:35])([CH2:28][CH2:29][C:30]([O:32][CH2:33][CH3:34])=[O:31])[O:26][CH2:25]1.[H-].[Na+]>O1CCCC1>[CH3:35][C:27]1([CH2:28][CH:29]([CH2:2][C:3]2[CH:8]=[CH:7][C:6]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[CH:5][CH:4]=2)[C:30]([O:32][CH2:33][CH3:34])=[O:31])[O:26][CH2:25][CH2:24][O:36]1

Komponenten

5

Versuchsvorschrift

A mixture of about 33 g of 1-(bromomethyl)-4-(tetradecyloxy)benzene, about 16.2 g of ethyl levulinate ethylene ketal, about 4.54 g of about 50% sodium hydride and about 350 ml of tetrahydrofuran was refluxed with stirring, under argon for about 18 hours and then filtered through celite. The solvent was removed and the residue was dissolved in ether. The ether solution was washed with aqueous monobasic sodium phosphate, dried and the solvent removed. The residue was subjected to high performance liquid chromatography (HPLC), using the system hexane:ethyl acetate (about 9:1), giving about 22.1 g of the desired title compound as a light yellow oil).

Aufarbeitung

  1. temperaturewas refluxed
  2. filtrationfiltered through celite
  3. customThe solvent was removed
  4. dissolutionthe residue was dissolved in ether
  5. washThe ether solution was washed with aqueous monobasic sodium phosphate
  6. customdried
  7. customthe solvent removed

Quellen und Nachweise

ORD-Eintrag
ord-95bfe5bf32f649c2b074aa3df909609f
Quelldatensatz
uspto-grants-1987_02
Patentnummer
US04640913

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