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Ethanolysis products from Douglas fir

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Title Ethanolysis products from Douglas fir
Names Fujii, Michihiro (creator)
Kurth, E. F. (advisor)
Date Issued 1965-08-13 (iso8601)
Note Graduation date: 1966
Abstract Douglas fir bark fines which contained 74.8 percent
of Klason lignin and 70.2 percent of one percent sodium
hydroxide solubility and decayed Douglas fir wood which
contained 53.9 percent of Klason lignin were subjected to
ethanolysis. A slight modification of the Hibbert's
ethanolysis procedure was used. The monomeric compounds
present in the reaction products were then examined.
Two fractions of ethyl ether soluble oil were obtained
from both bark and wood samples, which were mixtures of
monomeric compounds produced by the ethanolysis reaction.
One, which was designated "PE" fraction, was obtained by
an ether extraction of a tar-like water insoluble substance
of the ethanolysis products, and the other one designated
"LE" fraction was obtained by the ether extraction of a
water solution of the water soluble ethanolysis product.
Two dimensional paper partition chromatography of these
ether soluble oils demonstrated the presence of 12 compounds
in the bark "PE" fraction, four compounds in the bark "LE"
fraction and nine compounds in the wood "LE" fraction. The
wood "PE" fraction gave the same chromatogram as the wood
"LE". In the wood "LE", the typical Hibbert's monomers,
1-ethoxy-1-guaiacyl-2-propanone, 2-ethoxy-1-guaiacyl-lpropanone,
guaiacyl-acetone, vanilloyl-acetyle, vanillin,
and vanillic acid were identified. Ethyl ferulate was isolated
from the bark "PE", which was the only C₆-C₃, phenyl
propane type compound obtained from the ethanolysis of the
bark fines sample. Ethyl protocatechuate, protocatechuic
acid, and vanillic acid were isolated from the bark "PE"
and "LE". Ethyl vanillate was isolated from the bark "LE".
Identification of the esters was confirmed by comparison
with authentic samples prepared by synthesis.
From these results, it was concluded that the major
monomeric compounds which were produced by the ethanolysis
reaction of the bark fines were ferulic acid, protocatechuic
acid, and vanillic acid. This indicates that the building
units of the bark phenolic acid molecule are different from
those in the lignin from wood.
Genre Thesis/Dissertation
Topic Bark
Identifier http://hdl.handle.net/1957/47867

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