تفاعل #564656
ord-32316cee98584da7a6044fcbc462067b
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.DISTILLATIONexcess pyrrolidine was distilled off at reduced pressure
- 2أخرىto obtain an oil phase
- 3workup.ADDITIONwas added
- 4تجفيفthe ether phase was dried
- 5أخرىevaporated to dryness under reduced pressure
- 6أخرىThe oil residue was chromatographed over silica
- 7غسيلeluted with ethyl acetate containing 5% of triethylamine
الإجراء التجريبي
A solution of 10.8 ml of pyrrolidine in 6.75 g of 2,3-epoxy-indane [described by Mousseron et al., Bull. de Soc. Chim. de France, 1946, p. 629-630] was slowly added to 10.8 ml of demineralized water and after increasing the temperature to 65° C., the mixture was stirred for 90 minutes at 65° C. 20 ml of demineralized water were then added and excess pyrrolidine was distilled off at reduced pressure to obtain an oil phase and an aqueous phase. The aqueouse phase was saturated with sodium chloride and 1 ml of 32% sodium hydroxide was added thereto. The mixture was extacted with ether and the ether phase was dried and evaporated to dryness under reduced pressure. The oil residue was chromatographed over silica and eluted with ethyl acetate containing 5% of triethylamine to obtain 8.81 g of trans (±) 2,3-dihydro-1-(pyrrolidin-1-yl)-1H-inden-2-ol.