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THE USE OF GRIGNARD REAGENT IN PHEROMONE SYNTHESIS FOR PALM WEEVIL (<i>Rhynchorus, Sp</i>)
Author(s) -
Warsito Warsito,
Edi Priyo Utomo,
Achmad Ashadi,
Satriyo Santosa
Publication year - 2010
Publication title -
indonesian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.273
H-Index - 14
eISSN - 2460-1578
pISSN - 1411-9420
DOI - 10.22146/ijc.21878
Subject(s) - chemistry , pheromone , weevil , reagent , magnesium bromide , olfactometer , grignard reagent , grignard reaction , sex pheromone , bromide , acetogenin , organic chemistry , magnesium , botany , attraction , biology , linguistics , philosophy , annonaceae
In an integrated controlling system of palm weevil, using of synthetic feromoid is strickly needed. The research is aimed to synthesize pheromone which secreted by the weevil, e.g. 4-methyl-5-nonanol (R. ferrugineus) and 3-methyl-4-octanol (R. schach) through Grignard reagent which formed in situ. The synthesis was proceded by retrosynthesis to determine the precursor, valeraldehyde. The precursor was reacted with Grignard reagent of sec-amyl magnesium bromide (R. ferrugenieus) and secbutyl magnesium bromide (R. shach) which made in situ. Characterization of the synthetic molecular pheromone was performed by Gas Chromatography-mass spectroscopy and Fourier Transformed Infra Red. The bioassay of the molecule was carried out by olfactometer. The result showed that the conversion of the reactions were 51,28% (4-methyl-5-nonanol) and 85.90% (3-methyl-4-octanol). The character of physico-chemical and bioactivity of the synthetic pheromone are identic with natural pheromones.

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