Piperic acid
Names
Preferred IUPAC name
(2E ,4E )-5-(2H -1,3-Benzodioxol-5-yl)penta-2,4-dienoic acid
Identifiers
ChEBI
ChEMBL
ChemSpider
EC Number
MeSH
C017637
UNII
InChI=1S/C12H10O4/c13-12(14)4-2-1-3-9-5-6-10-11(7-9)16-8-15-10/h1-7H,8H2,(H,13,14)/b3-1+,4-2+
N Key: RHBGITBPARBDPH-ZPUQHVIOSA-N
N InChI=1/C12H10O4/c13-12(14)4-2-1-3-9-5-6-10-11(7-9)16-8-15-10/h1-7H,8H2,(H,13,14)/b3-1+,4-2+
Key: RHBGITBPARBDPH-ZPUQHVIOBF
C1OC2=C(O1)C=C(C=C2)/C=C/C=C/C(=O)O
Properties
C 12 H 10 O 4
Molar mass
218.208 g·mol−1
Boiling point
decomposes
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
Piperic acid is a chemical often obtained by the base -hydrolysis of the alkaloid piperine [ 1] from black pepper ,[ 2] followed by acidification of the corresponding salt . Piperic acid is an intermediate in the synthesis of other compounds such as piperonal , and as-such may be used to produce fragrances , perfumes flavorants and drugs as well as other useful compounds.
Preparation
Piperic acid can be prepared from the commercially-available alkaloid piperine , a cyclic amide containing a piperidine group, by reacting it with a hydroxide such as potassium hydroxide , then acidifying the formed piperate salt with hydrochloric acid or another acid. The toxic compound piperidine is given off during the base-hydrolysis of piperine and as-such, safety precautions should be taken.
Reactions
Reaction of piperic acid with strong oxidizers such as potassium permanganate or ozone , or a halogen such as bromine followed by sodium hydroxide causes oxidative cleavage of the double-bonds, yielding piperonal and piperonylic acid .[ 3] Piperonal has many uses in industry and is itself a precursor to a good subsection of other chemicals. On reduction with sodium amalgam piperic acid forms α- and β-dihydropiperic acid , C12 H12 O4 , and the latter can take up two further atoms of hydrogen to produce tetrahydropiperic acid .
See also
References