TY - JOUR
T1 - A Short Method for the Synthesis of Hydroxyoleic Acids
AU - IMPERIO, DANIELA
AU - Morelli, Laura
AU - PANZA, Luigi
N1 - Publisher Copyright:
© 2020 AOCS
PY - 2021
Y1 - 2021
N2 - Enzymatic or microbiological oxidation of oleic acid can afford azelaic acid as a building block for bioplastics. However, during the oxidation, the formation of hydroxylated byproducts is observed. To better follow the oxidation reaction, the availability of reference compounds is of great importance. To this aim, the synthesis of a series of oleic acids hydroxylated at ω ‐ 1, ω ‐ 2, ω ‐ 3 positions is described without the use of protecting groups. The final products are obtained by partial lactone reduction to hydroxyaldehyde followed by Grignard addition, selective oxidation of the primary hydroxyl group, and Wittig reaction.
AB - Enzymatic or microbiological oxidation of oleic acid can afford azelaic acid as a building block for bioplastics. However, during the oxidation, the formation of hydroxylated byproducts is observed. To better follow the oxidation reaction, the availability of reference compounds is of great importance. To this aim, the synthesis of a series of oleic acids hydroxylated at ω ‐ 1, ω ‐ 2, ω ‐ 3 positions is described without the use of protecting groups. The final products are obtained by partial lactone reduction to hydroxyaldehyde followed by Grignard addition, selective oxidation of the primary hydroxyl group, and Wittig reaction.
KW - Hydroxyoleic acid Macrolactone TEMPO Grignard Natural products
KW - Hydroxyoleic acid Macrolactone TEMPO Grignard Natural products
UR - https://iris.uniupo.it/handle/11579/118799
U2 - 10.1002/aocs.12454
DO - 10.1002/aocs.12454
M3 - Article
SN - 0003-021X
VL - 98
SP - 157
EP - 162
JO - JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
JF - JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
IS - 2
ER -