반응 #2383776

ord-aa907a7fc89748ba9a82338fba49a31d

반응 방정식

OC1(c2ccccc2-c2ccccc2)c2cc3ccccc3cc2C(O)(c2ccccc2-c2ccccc2)c2cc3c(ccc4ccccc43)cc21
8,15-bis(p-biphenylyl)-8,15-dihydro-8,15-dihydroxybenzo[a]-pentacene
I
hydrogen iodide
O=C([O-])O.[Na+]
sodium hydrogencarbonate
c1ccc(-c2ccccc2-c2c3cc4ccccc4cc3c(-c3ccccc3-c3ccccc3)c3cc4c(ccc5ccccc54)cc23)cc1
deep purple amorphous solid
수율 51.0%
c1ccc(-c2ccccc2-c2c3cc4ccccc4cc3c(-c3ccccc3-c3ccccc3)c3cc4c(ccc5ccccc54)cc23)cc1
8,15-bis(p-biphenylyl)benzo[a]pentacene
수율 51.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe obtained mixture was stirred for 10 minutes
  2. 2
    기타The formed precipitates
  3. 3
    기타were separated by filtration
  4. 4
    세척washed once with ion-exchanged water, once with a saturated aqueous solution of sodium disulfite
  5. 5
    기타The washed precipitates
  6. 6
    기타were dried
  7. 7
    온도under heating at a reduced pressure and 0.84 g (the yield: 51%) of a light purple solid of 8,15-bis(p-biphenylyl)benzo[a]pentacene
  8. 8
    기타was obtained
  9. 9
    기타The obtained product was purified by sublimation at 320° C. under 4.0×10−6 Torr for 2 hours

실험 절차

In 150 ml of isopropyl ether and 75 ml of dichloromethane, 1.5 g (2.3 mmole) of 8,15-bis(p-biphenylyl)-8,15-dihydro-8,15-dihydroxybenzo[a]-pentacene was suspended. To the obtained suspension, 40 ml of a 57% aqueous solution of hydrogen iodide was added under the refluxing condition and the obtained mixture was stirred for 5 minutes. After the reaction was completed, the reaction solution was added to 500 ml of a saturated aqueous solution of sodium hydrogencarbonate and the obtained mixture was stirred for 10 minutes. The formed precipitates were separated by filtration and washed once with ion-exchanged water, once with a saturated aqueous solution of sodium disulfite and then three times with ion-exchanged water. The washed precipitates were dried under heating at a reduced pressure and 0.84 g (the yield: 51%) of a light purple solid of 8,15-bis(p-biphenylyl)benzo[a]pentacene was obtained. The obtained product was purified by sublimation at 320° C. under 4.0×10−6 Torr for 2 hours and 450 mg of a deep purple amorphous solid was obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06489046B1uspto-grants-2002_12