반응 #69863

ord-5af76c94f69b496baa9aedebfd8933d8

반응 방정식

O=C([O-])O.[Na+]
NaHCO3
OCc1cccc(-c2ncccn2)c1
(3-(pyrimidin-2-yl)phenyl)methanol
O=P(Br)(Br)Br
POBr3
BrCc1cccc(-c2ncccn2)c1
title compound
수율 80.5%
BrCc1cccc(-c2ncccn2)c1
2-(3-(bromomethyl)phenyl)pyrimidine
수율 80.5%

용매

반응 조건

온도
60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was cooled to rt
  2. 2
    추출extracted with ethyl acetate (2×)
  3. 3
    건조The combined organic layers were dried over anhydrous Na2SO4
  4. 4
    여과filtered
  5. 5
    농축concentrated under reduced pressure
  6. 6
    기타The residue was purified by flash-column chromatography over silicagel (eluent: gradient 5%-40% ethyl acetate/heptane)

실험 절차

To a stirred solution of (3-(pyrimidin-2-yl)phenyl)methanol [892502-12-4] (2.48 g, 12.92 mmol) in THF (25 mL), POBr3 (4.81 g, 16.79 mmol) was added and the mixture was heated at 60° C. for 90 min. The mixture was cooled to rt, poured into saturated aqueous NaHCO3 solution and extracted with ethyl acetate (2×). The combined organic layers were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash-column chromatography over silicagel (eluent: gradient 5%-40% ethyl acetate/heptane) to yield the title compound (2.59 g, 80%). [1H NMR (400 MHz, DMSO-d6) ♀ ppm 8.92 (d, J=5.0 Hz, 2H), 8.48 (t, J=1.6 Hz, 1H), 8.32 (dt, J=7.7, 1.4 Hz, 1H), 7.58-7.62 (m, 1H), 7.49-7.54 (m, 1H), 7.47 (t, J=4.8 Hz, 1H), 4.82 (s, 2H); LCMS RtA=1.04, [M+H]+=249.2/251.2].

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08530648B2uspto-grants-2013_09