반응 #1062

ord-29bdac8cd38e44e3a6167a6148c0ca92

반응 방정식

c1ccc(Oc2ccc(C3CCNCC3)cc2)cc1
compound ( 4 )
c1ccc(Oc2ccc(C3CCNCC3)cc2)cc1
4-(4-phenoxyphenyl)piperidine
N#CCCl
chloroacetonitrile
[I-].[Na+]
sodium iodide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
N#CCN1CCC(c2ccc(Oc3ccccc3)cc2)CC1
compound ( 26 )
수율 91.0%
N#CCN1CCC(c2ccc(Oc3ccccc3)cc2)CC1
1-cyanomethyl-4-(4-phenoxyphenyl)piperidine
수율 91.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도This was then heated
  2. 2
    온도at reflux for 2 hours
  3. 3
    추출extraction
  4. 4
    기타The extract was dried
  5. 5
    여과filtered
  6. 6
    농축concentrated under reduced pressure
  7. 7
    기타to obtain a residue which
  8. 8
    기타was then purified by silica gel column chromatography (methylene chloride:methanol =30:1)

실험 절차

To an 8 ml dimethylformamide solution of 300 mg of the compound (4) synthesized in Reference Example 4 were added 93 mg of chloroacetonitrile, 355 mg of sodium iodide, and 196 mg of potassium carbonate. This was then heated at reflux for 2 hours. To the reaction was added 10 ml of ice water, then extraction was performed with ethyl acetate. The extract was dried, filtered, then concentrated under reduced pressure to obtain a residue which was then purified by silica gel column chromatography (methylene chloride:methanol =30:1) to obtain the above-identified compound (26) in an amount of 313 mg (yield of 91%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723475uspto-grants-1998_03