تفاعل #1994257

ord-cb8ae7d0ebf94ea1863ca1397fcdf327

معادلة التفاعل

c1ccc2c(c1)Cc1ccccc1N2
9,10-dihydroacridine
Brc1ccc(-c2ccccc2)cc1
4-bromobiphenyl
c1ccc(-c2ccc(N3c4ccccc4Cc4ccccc43)cc2)cc1
10-(biphenyl-4-yl)-9,10-dihydroacridine
المردود 70.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONThen, NaOBut (9.4 g, 97.8 mmol) was added
  2. 2
    غسيلwas washed with MC
  3. 3
    أخرىThe filtrate was evaporated under a reduced pressure
  4. 4
    أخرىto remove the solvent
  5. 5
    أخرىThe residue was then purified by silica gel column chromatography (methylene chloride/n-hexane (1/10))

الإجراء التجريبي

The obtained 9,10-dihydroacridine (11.8 g, 65.2 mmol) and 4-bromobiphenyl (18.2 g, 78.2 mmol) were dissolved in toluene (500 mL). Then, Pd2(dba)3 (1.4 g, 1.3 mmol) was added thereto under a nitrogen atmosphere. Then, NaOBut (9.4 g, 97.8 mmol) was added thereto, and (t-Bu)3P (1.6 ml, 2.6 mmol) was introduced to the resultant solution. The resultant mixture was reflux-stirred for 5 hours. The completion of the reaction was identified by a TLC. After the reaction was completed, the mixture was cooled to room temperature. The resultant solution was poured onto a thin silica pad so as to perform a short chromatography, and then was washed with MC. The filtrate was evaporated under a reduced pressure to remove the solvent. The residue was then purified by silica gel column chromatography (methylene chloride/n-hexane (1/10)) to obtain 10-(biphenyl-4-yl)-9,10-dihydroacridine compound (pale yellow solid, 15.3 g, yield 70%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08597802B2uspto-grants-2013_12