تفاعل #2025283

ord-ba372973847a4f07bac72a42048c0a1d

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىreacted for 2 hours
  2. 2
    استخلاصextracted with 200 ml of toluene
  3. 3
    أخرىseparated
  4. 4
    غسيلwashed with, in the order, 1N aqueous solution of hydrochloric acid, water, 5% aqueous solution of sodium bicarbonate and water
  5. 5
    تجفيفdried on anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONAfter the solvent was distilled out under the reduced pressure
  7. 7
    أخرىthe resulting residue was purified by silica gel column chromatography (eluent: toluene-ethyl acetate)

الإجراء التجريبي

2.56 (10 millimols) of (+)-3-methyl-3-(4-benzyloxyphenyl)propanol (XI-1) obtained in Preparation Example (starting material compound (V)) 1, was dissolved in 20 ml of pyridine and 1.38 g (13 millimols) of butyrylchloride was added at 30°-40° C. and reacted for 2 hours. The reaction mixture was poured into 200 ml of water and extracted with 200 ml of toluene and separated and then washed with, in the order, 1N aqueous solution of hydrochloric acid, water, 5% aqueous solution of sodium bicarbonate and water, and thereafter dried on anhydrous magnesium sulfate. After the solvent was distilled out under the reduced pressure, the resulting residue was purified by silica gel column chromatography (eluent: toluene-ethyl acetate) to provide 3.1 g (yield: 95%) of (+)-4-benzyloxy-1-(1-methyl-3-butyryloxypropyl)benzene (VIII-9).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05693251uspto-grants-1997_12