تفاعل #51201

ord-f9a00c7c17134bd8a61fcb3d6e21e6e3

الكواشف

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe catalyst was filtered through a pad of Arbocel
  2. 2
    أخرىthe filtrate evaporated to low (5 ml) volume
  3. 3
    workup.DISSOLUTIONThe remaining liquid was dissolved in EtOAc (30 ml)
  4. 4
    غسيلwashed with water
  5. 5
    تجفيفThe organic layer was dried over MgSO4
  6. 6
    أخرىevaporated to a pale yellow oil

الإجراء التجريبي

4-Chromanol (Aldrich) (2.77 g, 18.4 mmol) was taken up in acetic anhydride (3.5 ml, 36.9 mmol) and acetic acid (30 ml) and refluxed for 3 h, and then allowed to cool to room temperature over 16 h. 10% w/w Pd/C was then added to the solution and the whole hydrogenated at 40 p.s.i. hydrogen pressure for 16 h. The catalyst was filtered through a pad of Arbocel and the filtrate evaporated to low (5 ml) volume. The remaining liquid was dissolved in EtOAc (30 ml) and washed with water, then NaHCO3 solution (100 ml of each). The organic layer was dried over MgSO4 and evaporated to a pale yellow oil. This oil was columned in 10% EtOAc/pentane to give the title product (2.1 g, 85%);

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849649B2uspto-grants-2005_02