반응 #94953

ord-93eec3e9667745f9b5688539be76b279

반응 방정식

[Cl-].[NH4+]
ammonium chloride
O
water
N#Cc1ccc(Br)cc1
4-bromobenzonitrile
CN1CCC(Cl)CC1
4-chloro-1-methylpiperidine
[Mg]
magnesium
CN1CCC(C(=O)c2ccc(Br)cc2)CC1
(4-bromophenyl)-(1-methyl-4-piperidinyl)methanone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled (10°-15° C.) Grignard-complex
  2. 2
    기타previously prepared
  3. 3
    workup.STIRRINGUpon completion, stirring
  4. 4
    온도at reflux temperature
  5. 5
    추출The product is extracted with methylbenzene
  6. 6
    기타The extract is dried
  7. 7
    여과filtered
  8. 8
    기타evaporated
  9. 9
    기타The residue is purified by column-chromatography over silica gel using
  10. 10
    workup.ADDITIONa mixture of trichloromethane and methanol (95:5 by volume) as eluent
  11. 11
    기타The pure fractions are collected
  12. 12
    기타the eluent is evaporated

실험 절차

To a stirred and cooled (10°-15° C.) Grignard-complex, previously prepared starting from 13.5 parts of 4-chloro-1-methylpiperidine and 2.4 parts of magnesium in 68 parts of tetrahydrofuran, is added dropwise a solution of 10 parts of 4-bromobenzonitrile in 22 parts of tetrahydrofuran. Upon completion, stirring is continued for 1 hour at reflux temperature. The reaction mixture is decomposed by pouring onto a mixture of 50 parts of ammonium chloride in 250 parts of water. The product is extracted with methylbenzene. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 10 parts of (4-bromophenyl)-(1-methyl-4-piperidinyl)methanone as a residue.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04342870uspto-grants-1982_08