تفاعل #2439932

ord-c9fe9cd5547948c48f27a6922e597452

معادلة التفاعل

CC1(C)c2cc(B(O)O)ccc2-c2ccc(B(O)O)cc21
9,9-dimethylfluorene-2,7-diboronic acid
CC1(C)c2cc(I)ccc2-c2ccc(I)cc21
2,7-diiodo-9,9-dimethyl fluorene
O=C([O-])[O-].[Na+].[Na+]
Na2CO3
Cl
HCl
CC1(C)c2cc(B(O)O)ccc2-c2ccc(B(O)O)cc21
9,9-dimethylfluorene-2,7-diboronic acid
CC1(C)c2cc(I)ccc2-c2ccc(I)cc21
2,7-diiodo-9,9-dimethyl fluorene
c1ccc2c(c1)Cc1ccccc1-2
fluorene

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىaccording to synthesis example 1
  2. 2
    أخرىa Suzuki reaction
  3. 3
    workup.ADDITIONby adding
  4. 4
    درجة الحرارةThereafter, after refluxing for 7 hr
  5. 5
    غسيلby washing a toluene phase with water until neutrality
  6. 6
    أخرىis obtained
  7. 7
    تجفيفAfter drying with sodium sulfate
  8. 8
    ترشيحby filtering
  9. 9
    workup.DISTILLATIONdistilling the solvent away
  10. 10
    أخرىa crude product is obtained
  11. 11
    غسيلAfter washing with substantially 100 ml of methanol
  12. 12
    أخرىa colorless crystal is obtained
  13. 13
    أخرىto remove original components
  14. 14
    أخرىby recrystallizing

الإجراء التجريبي

With 9,9-dimethylfluorene-2,7-diboronic acid and 2,7-diiodo-9,9-dimethyl fluorene, which are synthesized according to synthesis example 1, a Suzuki reaction is carried out. Under a nitrogen atmosphere, tetrakis(triphenylphosphine)palladium(0) (1.0 mmol) is dissolved in THF (50 ml), followed by adding thereto 2,7-diiodo-9,9-dimethyl fluorene (50 mmol), a solution of 2M Na2CO3 (50 ml) and 9,9-dimethylfluorene-2,7-diboronic acid (25 mmol)/THF (100 ml) in this order. Thereafter, after refluxing for 7 hr, a reaction is brought to an end. The solution is cooled to room temperature, followed by substituting with toluene and adding substantially 30 ml of 1N HCl, further followed by washing a toluene phase with water until neutrality is obtained. After drying with sodium sulfate, followed by filtering and distilling the solvent away, and thereby a crude product is obtained. After washing with substantially 100 ml of methanol, a colorless crystal is obtained. Furthermore, by passing through a short column from hexane/ethyl acetate to remove original components, finally followed by recrystallizing, and thereby fluorene trimer (20 mmol) is obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07749618B2uspto-grants-2010_07