تفاعل #336455
ord-41df85ac0239484fb58d77371c74847d
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المعالجة
- 1workup.ADDITIONAfter the dropwise addition the mixture
- 2أخرىThe reaction mixture was evaporated in a rotary evaporator
- 3أخرىthe residue was chromatographed on 400 g of neutral aluminium oxide (activity grade III) with hexane:ethyl acetate (7:3)
- 4أخرىThe yellowish oil obtained
- 5أخرىThe colorless crystals which separate
- 6ترشيحwere filtered off under suction
- 7غسيلwashed with ether
- 8أخرىrecrystallized from acetone
الإجراء التجريبي
A mixture of 2.5 g of N,N-dimethyl-6-amino-1-hexanol (Bull. Soc. Chim. France 1975, 2315), 3.4 g of 4-hydroxybenzophenone (Beilstein 8 (III), 1263), 4.5 g of triphenylphosphine and 140 ml of tetrahydrofuran was treated slowly at 20° with a solution of 2.7 ml of diethyl azodicarboxylate in 15 ml of tetrahydrofuran. After the dropwise addition the mixture was stirred at room temperature for a further 1 hour. The reaction mixture was evaporated in a rotary evaporator and the residue was chromatographed on 400 g of neutral aluminium oxide (activity grade III) with hexane:ethyl acetate (7:3). The yellowish oil obtained was dissolved in 25 ml of ether, whereupon the solution was treated with 25 ml of a 10 percent solution of hydrogen chloride in ether. The colorless crystals which separate were filtered off under suction, washed with ether and recrystallized from acetone. There were obtained 1.93 g (31%) of 4-[(6-dimethylamino)hexyl)oxy]benzophenone hydrochloride of m.p. 121°.