Réaction #2467919

ord-6339baad790447f18a3e125655c1c6c0

Équation de réaction

CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)Cl
z,z,z-octadeca-6,9,12-trienoyl chloride
Cc1ncc(CO)c(C=O)c1O.Cl
pyridoxal hydrochloride
CCN(CC)CC
triethylamine
CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)OCc1cnc(C)c(O)c1C=O
2-methyl-3-hydroxy-4-formyl-5-(z,z,z-octadeca-6,9,12-trienoyloxy)methyl pyridine

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Concentrationthe mixture was concentrated
  2. 2
    Autrepurified by flash chromatography (ethyl acetate/hexane)

Mode opératoire

A solution of z,z,z-octadeca-6,9,12-trienoyl chloride (800 mg, 2.7 mmol) in methylene chloride (10 ml) was added slowly dropwise to a mixture of pyridoxal hydrochloride (500 mg, 2.45 mmol), triethylamine (1 ml, 7.2 mmol) and 4-(N,N-dimethylamino)pyridine (few mg, catalytic amount) in methylene chloride (20 ml) at 0° C. under nitrogen. On completion, as indicated by tlc, the mixture was concentrated and purified by flash chromatography (ethyl acetate/hexane), yielding 2-methyl-3-hydroxy-4-formyl-5-(z,z,z-octadeca-6,9,12-trienoyloxy)methyl pyridine as a colourless oil which subsequently solidified.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE043632E1uspto-grants-2012_09