Réaction #6290

ord-71e3ae6057b24905aebe514e2d6cc7ed

Équation de réaction

COc1cc(C=O)ccc1O
vanillin
BrCCCCCCCCCCBr
1,10-dibromodecane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)=O
acetone
COc1cc(C=O)ccc1OCCCCCCCCCCOc1ccc(C=O)cc1OC
compound
COc1cc(C=O)ccc1OCCCCCCCCCCOc1ccc(C=O)cc1OC
1,10-Di(2-methoxy-4-formylphenoxy)decane

Solvants

Conditions de réaction

Température
5°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurecooled
  2. 2
    workup.DISSOLUTIONAfter the salts had dissolved
  3. 3
    FiltrationThe solid product was filtered
  4. 4
    Lavagewashed twice with water
  5. 5
    Autrerecrystallized (still wet) from 250 ml of ethanol
  6. 6
    TempératureCooling to 25° C.

Mode opératoire

A slurry of 13.42 g of vanillin, 11.99 g of 1,10-dibromodecane, 6.16 g of anhydrous potassium carbonate and 300 ml of acetone was refluxed with stirring for 48 h, cooled and diluted with 400 ml of water. After the salts had dissolved, the mixture was chilled overnight at 5° C. The solid product was filtered, washed twice with water and recrystallized (still wet) from 250 ml of ethanol. Cooling to 25° C. gave 4.75 g of compound mp 93°-102° C., wetting at 65° C. (Further cooling of the mother liquors to 5° C. furnished 3.5 g of very impure materials, mp 55°-65° C.). Another recrystallization from 130 ml of ethanol raised the mp to 103°-105° C., slight wetting at 99° C.; 3.16 g.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05247055uspto-grants-1993_09