반응 #975886

ord-799e27180346445d89d812bd797cbb26

반응 방정식

CC(=O)[O-].[NH4+]
ammonium acetate
O=C(C[n+]1ccccc1)c1ccc(Br)cc1.[I-]
4-bromophenacylpyridinium iodide
O=Cc1ccc2ccccc2c1
2-naphthoaldehyde
CC(=O)c1ccccn1
2-acetylpyridine
CO.[Na+].[OH-]
NaOH methanol
Brc1ccc(-c2cc(-c3ccc4ccccc4c3)cc(-c3ccccn3)n2)cc1
6-(4-bromophenyl)-4-(naphthalen-2-yl)-[2,2′]bipyridine
수율 23.0%

반응 조건

온도
-5°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe whole was stirred at −5° C. for 2 hours
  2. 2
    workup.STIRRINGthe whole was stirred at 55° C. for 2 days
  3. 3
    온도After cooling to room temperature
  4. 4
    여과the resulting crude product was collected by filtration
  5. 5
    세척washed with methanol
  6. 6
    기타dried under reduced pressure at 70° C. for 12 hours

실험 절차

Subsequently, 6.0 g of 2-naphthoaldehyde, 4.7 g of 2-acetylpyridine, and 40 ml of methanol were added and the whole was cooled to −5° C. under stirring. 62 ml of a 3 wt % NaOH/methanol solution was added dropwise thereto and the whole was stirred at −5° C. for 2 hours. Then, the reaction was further carried out at the same temperature for 2 days. 37.0 g of ammonium acetate, 15.5 g of the above 4-bromophenacylpyridinium iodide, and 100 ml of methanol were added to the reaction solution and the whole was stirred at 55° C. for 2 days. After cooling to room temperature, the resulting crude product was collected by filtration, washed with methanol, and then dried under reduced pressure at 70° C. for 12 hours to obtain 3.8 g (yield 23%) of 6-(4-bromophenyl)-4-(naphthalen-2-yl)-[2,2′]bipyridine as a gray powder.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08252431B2uspto-grants-2012_08