Reaktion #928305

ord-b0d5989124334152b46aa14de0f2b988

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe compound (IV) was prepared
  2. 2
    SonstigeThe product was purified by chromatography
  3. 3
    workup.ADDITIONmix
  4. 4
    SonstigeThe intermediate fractions were collected
  5. 5
    Sonstigethe solvent was evaporated under reduced pressure
  6. 6
    Sonstigea 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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06369260B1uspto-grants-2002_04