反応 #1483119

ord-7a0bfa03501545beb2acd206e38eb78f

反応方程式

Cl
HCl
c1ccncc1
pyridine
COc1ccccc1-c1ccc2ccc3cccnc3c2n1.Cl.[Cl-]
2-(2-methoxyphenyl)-1,10-phenanthroline hydrochloride chloride
Oc1ccccc1-c1ccc2ccc3cccnc3c2n1
2-(2-Hydroxyphenyl)-1,10-Phenanthroline

反応条件

温度
140°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The resulting solution was heated on a sand bath
  2. 2
    workup.DISTILLATIONthe distillate collected in a Dean-Stark trap
  3. 3
    その他to rise back again to 215-220° C.
  4. 4
    workup.WAITheld at this temperature for 3 hours
  5. 5
    温度The solution was then cooled to 100° C.
  6. 6
    その他to precipitate a gummy solid
  7. 7
    ろ過The orange solid was filtered off
  8. 8
    洗浄washed well with water
  9. 9
    その他dried

実験手順

Concentrated HCl (17.6 mL) and pyridine (16 mL) were mixed together at room temperature. The resulting solution was heated on a sand bath while passing nitrogen over the surface of the solution and the distillate collected in a Dean-Stark trap. The internal temperature of the reaction was allowed to reach 215-220° C. over a 1 hour period. The solution was allowed to cool to 140° C. and 2-(2-methoxyphenyl)-1,10-phenanthroline hydrochloride chloride (6 g, 18.59 mMole) then added. With good stirring, the temperature of the resulting solution was allowed to rise back again to 215-220° C. and held at this temperature for 3 hours. The solution was then cooled to 100° C. and treated carefully with water (10 mL), then finally poured into an excess of water (70 mL) to precipitate a gummy solid. With good stirring, the pH of the solution was adjusted to 6-7 with solid Na2CO3. The orange solid was filtered off, washed well with water and dried. Yield of the 2-(2-hydroxyphenyl)-1,10-phenanthroline was 4.6 g.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08900722B2uspto-grants-2014_12