Reaktion #2667

ord-23ad7b54403248708606eeee9fbf6470

Reaktionsgleichung

COc1cc(C=O)cc(I)c1O
5-iodo vanillin
BrB(Br)Br
boron tribromide
O=Cc1cc(O)c(O)c(I)c1
expected product
Ausbeute 66.2%
O=Cc1cc(O)c(O)c(I)c1
3-iodo-4,5-dihydroxy benzaldehyde
Ausbeute 66.2%

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenwas then concentrated
  2. 2
    Temperaturcooled to 0° C.
  3. 3
    SonstigeThe crystallized product was separated out
  4. 4
    Waschenwashed with water
  5. 5
    Sonstigedried
  6. 6
    Sonstigecrystallized from an isopropanol

Vorschrift

37.2 g of 5-iodo vanillin (commercial) and 360 ml of dichloromethane were mixed together under nitrogen and the mixture was cooled to 0° C. 135 ml of a molar solution of boron tribromide in dichloromethane were added and the mixture stood for 16 hours at ambient temperature and was then concentrated, cooled to 0° C. and acidified. The crystallized product was separated out, washed with water, dried and crystallized from an isopropanol--water mixture (1-2 by volume) to obtain 23.4 g of the expected product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728828uspto-grants-1998_03