تفاعل #461546

ord-1f85c80fb2c64ac1ba8fb82c716ea1f2

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwere pumped at 250 bar and 60° C. through the imination reactor
  2. 2
    أخرىto top at 250 bar and 120° C.
  3. 3
    أخرىwas removed by distillation
  4. 4
    أخرىThe product from 16.7 hours was separated by fractional distillation on a 30 cm

الإجراء التجريبي

Example 1 was repeated using 2-butyl-2-ethyl-4-cyanobutanal as the starting material. To this end, 33.6 g per hour of 2-butyl-2-ethyl-4-cyanobutanal (purity 89.0%, 29.9 g, 0.165 mol) and 1344 ml (806 g, 47.4 mol) per hour of liquid ammonia were pumped at 250 bar and 60° C. through the imination reactor. The product stream was subsequently passed through the hydrogenation reactor from bottom to top at 250 bar and 120° C. while simultaneously passing 100 l(S.T.P.)/h (4.5 mol) of hydrogen through the reactor. The product stream was decompressed to atmospheric pressure and NH3 was removed by distillation. The product from 16.7 hours was separated by fractional distillation on a 30 cm packed column (3 mm glass rings), giving 166.8 g of 3-butyl-3-ethylpiperidine (b.p.=73° to 75° C./2 mmHg) and 267.5 g of 2-butyl- 2-ethylpentane-1,5-diamine (b.p.=105° C./2 mmHg). The diamine yield was 52.1% of theory.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05166443uspto-grants-1992_11