تفاعل #1880957
ord-921a8f6fd6574a2f83e8853db626757f
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةThe reaction mixture was then refluxed for 20 h
- 2درجة الحرارةafter cooling
- 3استخلاصextracted three times
- 4تجفيفThe combined ether extracts were dried over sodium sulfate
- 5أخرىfreed from solvent on a rotary evaporator
- 6workup.ADDITION400 ml of 2N hydrochloric acid were added
- 7درجة الحرارةthe mixture was refluxed for 20 h
- 8workup.ADDITIONThe mixture was then poured into 1.5 l of ice water
- 9استخلاصthe product was extracted four times
- 10غسيلeach time with 1.5 l of ether, and the combined ether extracts were washed with 1 l of water and 100 ml of saturated sodium chloride solution
- 11تجفيفAfter drying over sodium sulfate, concentration on a rotary evaporator and flash chromatography
الإجراء التجريبي
A solution of 69.0 g (234 mmol) of methyl 4-allyl-2-(ethoxycarbonylmethoxy)phenoxyacetate was added dropwise in the course of 2.5 h to a suspension of 12.0 g (500 mmol) of sodium hydride in 500 ml of tetrahydrofuran. The reaction mixture was then refluxed for 20 h and, after cooling, poured into 1.5 l of ice water. The resultant mixture was acidified to pH 2 with 2N hydrochloric acid and extracted three times, each time with 2 l of ether. The combined ether extracts were dried over sodium sulfate, freed from solvent on a rotary evaporator and taken up into 400 ml of ethanol. 400 ml of 2N hydrochloric acid were added and the mixture was refluxed for 20 h. The mixture was then poured into 1.5 l of ice water, the product was extracted four times, each time with 1.5 l of ether, and the combined ether extracts were washed with 1 l of water and 100 ml of saturated sodium chloride solution. After drying over sodium sulfate, concentration on a rotary evaporator and flash chromatography. (pentane/ether, 4:1, Rf=0.37) on silica gel, 20.0 g (42%) of 7-allylbenzo[b][1,4]dioxepin-3-one (1) were obtained as a colorless liquid.