반응 #629600

ord-534c0d146add497797903aa8ddf66e08

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도were heated
  2. 2
    workup.DISTILLATIONWhen ethyl bromide ceased distilling off (about 2 h) the remaining volatile by-products
  3. 3
    기타the triethylphosphite were removed from the mixture by distillation under vacuum
  4. 4
    기타The remaining oil was chromatographed on a column of silica gel with hexame-ethyl acetate (1:1) as eluant
  5. 5
    농축The combined fractions were concentrated under reduced pressure

실험 절차

In a round bottom flask equipped for distillation, 11.36 g (38.9 mmol) of 2-(3-bromopropyl)benzyl bromide and 6.46 (38.9 mmol) of freshly distilled triethylphosphite were heated with stirring at 100°-110° C. on an oil bath. When ethyl bromide ceased distilling off (about 2 h) the remaining volatile by-products and the triethylphosphite were removed from the mixture by distillation under vacuum. The remaining oil was chromatographed on a column of silica gel with hexame-ethyl acetate (1:1) as eluant. The combined fractions were concentrated under reduced pressure to yield 11.2 g (83%) of the product as a clear oil. IR(neat): 2985, 1496, 1450, 1391, 1252, 1162, 104, 967, 843, 802, 758 cm-1. 1H NMR(CDCl3) δ 1.2 (t, 6); 1.8-2.3 (m, 2H); 2.7-3.55 (m, 4H); 3.8-4.2 (m, 2H); 7.1-7.4 (m, 4H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04657899uspto-grants-1987_04