Reaktion #928305
ord-b0d5989124334152b46aa14de0f2b988
Reaktionsgleichung
Edukte
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeThe compound (IV) was prepared
- 2SonstigeThe product was purified by chromatography
- 3workup.ADDITIONmix
- 4SonstigeThe intermediate fractions were collected
- 5Sonstigethe solvent was evaporated under reduced pressure
- 6Sonstigea solid residue was obtained which
Vorschrift
The compound (IV) was prepared according to the procedure described in Example 1 for the synthesis of (XIX), starting from 5 g of the chloride of acetylsalicylic acid, 3.5 ml of TEA and 2.17 g of 1.10-decandiol. The product was purified by chromatography utilizing an eluent mix constituted by ethylether/hexane 7:3 (v/v). The intermediate fractions were collected, the solvent was evaporated under reduced pressure and a solid residue was obtained which, trirurated with isopropyl ether, produced 1.37 g of 1.10-decandiol bis-acetylsalicylate (IV) with m.p.=75° C.