Réaction #1747847

ord-83cf22de5eae44bd962548ea825fad60

Équation de réaction

CC(C)OB(OC(C)C)OC(C)C
triisopropyl borate
CCCCCC
hexane
[Li][CH2]CCC
n-butyllithium
Cl
hydrochloric acid
Brc1ccc(-c2cc3ccccc3c3ccccc23)cc1
9-(4-bromophenyl)phenanthrene
OB(O)c1ccc(-c2cc3ccccc3c3ccccc23)cc1
4-(9-phenanthrenyl)phenylboronic acid
Rendement 72.4%

Solvants

Conditions de réaction

Température
-60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGThen, the reaction mixture was stirred for two hours at −60 degrees C
  2. 2
    TempératureThe reaction solution was further cooled down to −60 degrees C
  3. 3
    TempératureSubsequently, the reaction mixture was warmed up to room temperature
  4. 4
    workup.STIRRINGstirred for 17 hours
  5. 5
    TempératureThe reaction mixture was cooled down to 0 degree C
  6. 6
    workup.STIRRINGstirred for one hour at room temperature
  7. 7
    AutreAfter the reaction
  8. 8
    SéchageAfter organic phase thereof was dried with magnesium sulfate
  9. 9
    workup.DISTILLATIONthe solvent was distilled away under reduced pressure
  10. 10
    AutreBy recrystallizing residue by toluene and hexane

Mode opératoire

Under an argon gas atmosphere, a mixture of 21.3 g (63.9 mmol) of 9-(4-bromophenyl)phenanthrene and 200 mL of dehydrated THF was cooled down to −60 degrees C., and added with 49.2 mL (76.7 mmol) of hexane solution of 1.56M n-butyllithium in drops while being stirred. Then, the reaction mixture was stirred for two hours at −60 degrees C. The reaction solution was further cooled down to −60 degrees C. and added with 36.1 g (192 mol) of triisopropyl borate in drops. Subsequently, the reaction mixture was warmed up to room temperature, and stirred for 17 hours. The reaction mixture was cooled down to 0 degree C. to be further added with solution of hydrochloric acid, and then stirred for one hour at room temperature. After the reaction, the reaction mixture was further added with toluene, so that aqueous phase thereof was eliminated. After organic phase thereof was dried with magnesium sulfate, the solvent was distilled away under reduced pressure. By recrystallizing residue by toluene and hexane, 13.8 g of 4-(9-phenanthrenyl)phenylboronic acid was obtained at an yield of 72%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08029697B2uspto-grants-2011_10