Réaction #52128

ord-8826021f3fe142c0834142035b884578

Équation de réaction

Oc1ccc(-c2nc(-c3ccc(Oc4ccccc4)cc3)nc(-c3ccc(Oc4ccccc4)cc3)n2)c(O)c1
2-(2,4-dihydroxyphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine
CCCCCCCCI
1-iodooctane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)CC(C)C
MIBK
CCCCCCCCOc1ccc(-c2nc(-c3ccc(Oc4ccccc4)cc3)nc(-c3ccc(Oc4ccccc4)cc3)n2)c(O)c1
2-(2-hydroxy-4-octyloxyphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine
Rendement 57.7%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas heated
  2. 2
    Températureto reflux for 3 hr
  3. 3
    Filtrationfiltered through Celite
  4. 4
    ConcentrationThe filtrate was concentrated under reduced pressure
  5. 5
    AutreThe residue thus obtained
  6. 6
    AutreThe material thus obtained
  7. 7
    Autrewas crystallized with acetone

Mode opératoire

A mixture of 5 gm 2-(2,4-dihydroxyphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine, 2.5 gm 1-iodooctane, 6.6 gm anhydrous potassium carbonate, 0.5 gm Aliquat 336 and 25 ml MIBK was heated to reflux for 3 hr. The reaction mixture was cooled to room temperature, diluted with methylene chloride, filtered through Celite. The filtrate was concentrated under reduced pressure. The residue thus obtained was passed through a silica gel column. The material thus obtained was crystallized with acetone to give 3.5 gm of pure 2-(2-hydroxy-4-octyloxyphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06855269B2uspto-grants-2005_02