تفاعل #2025283
ord-ba372973847a4f07bac72a42048c0a1d
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىreacted for 2 hours
- 2استخلاصextracted with 200 ml of toluene
- 3أخرىseparated
- 4غسيلwashed with, in the order, 1N aqueous solution of hydrochloric acid, water, 5% aqueous solution of sodium bicarbonate and water
- 5تجفيفdried on anhydrous magnesium sulfate
- 6workup.DISTILLATIONAfter the solvent was distilled out under the reduced pressure
- 7أخرىthe 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).