http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1316551-A1

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filingDate 2000-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ebb55c949b8e4d8200f8faacace5e54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10f5cf54744a219b7561d8a34f07060e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c080ddd2d4adbc269a955ce5ad7d2f74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be05531006874aa5cf3decd795564546
publicationDate 2003-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1316551-A1
titleOfInvention Process for preparing epoxy compounds, aromatic compositions containing the compounds, and drinks, perfumes, cosmetics, cigarettes, and tobaccos containing the compositions
abstract This invention provides a process for producing an epoxyncompound industrially advantageously at low cost in a short process.nFurthermore, this invention provides a novel fruity, camphoric,nfloral, amber or woody fragrance-, flavor- or scent-impartingncomposition containing said epoxy compound, and foods & drinks,nperfumes, cosmetics and tobaccos containing said composition. n In this invention, the epoxy compound can be produced bynletting an a-halocyclododecanone represented by the followingngeneral formula (1)n n(where X 1 denotes chlorine, bromine or iodine) and an organicnmagnesium compound represented by the following general formulan(2)n R 1 MgX 1 n(where R 1 denotes an alkyl group with 1 to 5 carbon atoms, alkenylngroup with 2 to 5 carbon atoms or alkynyl group with 2 to 5 carbonnatoms, and X 1 denotes chlorine, bromine or iodine) react with eachnother for Grignard reaction, hydrolyzing to obtain a halohydrinnrepresented by the following general formula (3) n n(where R 1 denotes an alkyl group with 1 to 5 carbon atoms, alkenylngroup with 2 to 5 carbon atoms or alkynyl group with 2 to 5 carbonnatoms; X 1 denotes chlorine, bromine or iodine; and the wavy linendenotes cis form, trans form or a mixture consisting of cis formnand trans form), and letting the halohydrin and a base react withneach other in the presence of an phase transfer catalyst or addingnan aprotic polar solvent for reaction.
priorityDate 2000-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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