تفاعل #336455

ord-41df85ac0239484fb58d77371c74847d

معادلة التفاعل

CN(C)CCCCCCO
N,N-dimethyl-6-amino-1-hexanol
O=C(c1ccccc1)c1ccc(O)cc1
4-hydroxybenzophenone
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCOC(=O)N=NC(=O)OCC
diethyl azodicarboxylate
Cl
hydrogen chloride
Cl.O=C(c1ccccc1)c1ccccc1
benzophenone hydrochloride

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter the dropwise addition the mixture
  2. 2
    أخرىThe reaction mixture was evaporated in a rotary evaporator
  3. 3
    أخرىthe residue was chromatographed on 400 g of neutral aluminium oxide (activity grade III) with hexane:ethyl acetate (7:3)
  4. 4
    أخرىThe yellowish oil obtained
  5. 5
    أخرىThe colorless crystals which separate
  6. 6
    ترشيحwere filtered off under suction
  7. 7
    غسيلwashed with ether
  8. 8
    أخرىrecrystallized 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°.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05214046uspto-grants-1993_05