반응 #6235

ord-8ddd5dd4e0684c5fbacd7457ef7264ca

반응 방정식

Oc1ccncc1
4-hydroxypyridine
O=C1c2ccccc2C(=O)N1CCCCBr
N-(4bromobutyl)phthalimide
C1CCC2=NCCCN2CC1
1,8-diazabicyclo[5.4.0]-7-undecene
O=C1c2ccccc2C(=O)N1CCCCOc1ccncc1
desired compound
수율 17.8%
O=C1c2ccccc2C(=O)N1CCCCOc1ccncc1
4-(4-phthalimidobutyloxy)pyridine
수율 17.8%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.DISTILLATIONAfter the solvent was distilled off
  2. 2
    workup.ADDITIONthe mixture was poured into water
  3. 3
    추출extracted with ethyl acetate
  4. 4
    세척The mixture was washed with water
  5. 5
    건조dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONthe solvent was distilled off
  7. 7
    기타The residue was purified by column chromatography (eluent: ethyl acetate)

실험 절차

To a solution of 4.76 g (50 mmol) of 4-hydroxypyridine and 15.52 g (55 mmol) of N-(4bromobutyl)phthalimide in 80 ml of DMF was added 8.23 ml (5 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene. The mixture was stirred at room temperature for 7 hours. After the solvent was distilled off, the mixture was poured into water and extracted with ethyl acetate. The mixture was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 2.63 g of the desired compound (yield: 17.2%, colorless crystals).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05246948uspto-grants-1993_09