Reaktion #1841204

ord-3b491246353d430d90c949081d47fb42

Reaktionsgleichung

O=S(=O)(O)O
sulfuric acid
Cc1ccccc1C
xylene
CCCCCCCCCCCCCCCCCCCCCC(=O)O
behenic acid
OC[C@@H](O)[C@@H](O)CO
erythritol
CCCCCCCCCCCCCCCCCCCCCC(=O)O[C@@H](CO)[C@@H](CO)OC(=O)CCCCCCCCCCCCCCCCCCCCC
solid
CCCCCCCCCCCCCCCCCCCCCC(=O)O[C@@H](CO)[C@@H](CO)OC(=O)CCCCCCCCCCCCCCCCCCCCC
Erythritol 2,3-Dibehenate

Lösungsmittel

Reaktionsbedingungen

Temperatur
145°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas equipped with a stirrer, a condenser and an addition funnel
  2. 2
    Temperaturto cool to room temperature
  3. 3
    SonstigeThe solid was removed by filtration
  4. 4
    Waschenthe liquid phase was washed with a saturated sodium bicarbonate aqueous solution and petroleum ether in sequence

Vorschrift

340 g (1 mol) behenic acid and 61 g (0.5 mol) erythritol were added into a 2 L three-neck flask which was equipped with a stirrer, a condenser and an addition funnel. To the flask was added 1 L xylene as a water carrier, followed by addition of a reaction catalyst sulfuric acid (32 g, 8 wt %). The mixture was refluxed at 145±2° C. for 22 hours. When the reaction was ended, the reaction system was allowed to cool to room temperature and stand for 2 hours. The solid was removed by filtration, and the liquid phase was washed with a saturated sodium bicarbonate aqueous solution and petroleum ether in sequence. 260 g solid product was obtained after drying by rotary evaporation. The product was erythritol 2,3-dibehenate as characterized by 1H NMR, and the purity was 91% as characterized by HPLC.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09169191B2uspto-grants-2015_10