تفاعل #1880956
ord-c3faba30857a46478bdd1e746f0cda60
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةAfter refluxing for 8 h
- 2درجة الحرارةafter a further 4 h of heating
- 3درجة الحرارةAfter a further 4 h under reflux
- 4ترشيحfiltering off the precipitate
- 5أخرىformed
- 6تركيزThe filtrate was concentrated on a rotary evaporator
- 7أخرىThe organic phase was separated off
- 8استخلاصthe aqueous phase was extracted three times
- 9تجفيفThe combined organic phases were dried over sodium sulfate
- 10تركيزconcentrated to dryness on a rotary evaporator
الإجراء التجريبي
12.8 g (225 mmol) of 95% pure sodium methoxide were introduced into a solution of 16.8 g (112 mmol) of 4-allylcatechol in 250 ml of methanol, with stirring, followed by 21 ml (225 mmol) of methyl bromoacetate. After refluxing for 8 h, a further 21 ml (225 mmol) of methyl bromoacetate were added, and, after a further 4 h of heating, a further 12.8 g (225 mmol) of sodium methoxide and a further 21 ml (225 mmol) of methyl bromoacetate. After a further 4 h under reflux, the mixture was worked up by adding 500 ml of ether and filtering off the precipitate formed. The filtrate was concentrated on a rotary evaporator and taken up in ether/water/saturated ammonium chloride solution (1:1:1). The organic phase was separated off, and the aqueous phase was extracted three times, each time with 200 ml of ether. The combined organic phases were dried over sodium sulfate and concentrated to dryness on a rotary evaporator. After flash chromatography (ether/pentane, 1:1, Rf=0.35) on silica gel, 21.4 g (65%) of methyl 4-allyl-2-(ethoxycarbonylmethoxy)phenoxyacetate were obtained.