반응 #366855

ord-1efc2d88839847949e671cd7816de0e3

반응 방정식

OCc1ccnc(Cl)c1
2-chloro-4-hydroxymethylpyridine
CNC
dimethylamine
CN(C)c1cc(CO)ccn1
4-hydroxymethyl-2-(dimethylamino)pyridine
수율 94.0%

용매

반응 조건

온도
200°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타(prepared
  2. 2
    온도to cool
  3. 3
    기타the mixture partitioned between saturated aqueous sodium bicarbonate solution and ethyl acetate
  4. 4
    기타The organic layer was separated
  5. 5
    건조dried (MgSO4)
  6. 6
    기타the volatiles removed by evaporation
  7. 7
    기타The residue was purified by column chromatography
  8. 8
    세척eluting with ethyl acetate

실험 절차

A mixture of 2-chloro-4-hydroxymethylpyridine (1.0 g, 7 mmol), (prepared as described for the starting material in Example 58), and dimethylamine (30 ml of a 30% solution in ethanol) was heated in a Carius tube for 16 hours at 200° C. The mixture was allowed to cool and the mixture partitioned between saturated aqueous sodium bicarbonate solution and ethyl acetate. The organic layer was separated, dried (MgSO4) and the volatiles removed by evaporation. The residue was purified by column chromatography eluting with ethyl acetate to give 4-hydroxymethyl-2-(dimethylamino)pyridine (1 g, 94%) as a yellow oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06362336B1uspto-grants-2002_03