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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fec576c38e34882531ca37d6b922bf42
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 2002-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e750472cf88b93a904c5b9d5239765d9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4656f165a48b05b56036ed177b29353e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_881115d9ccf118103614f0e78266ba4d
publicationDate 2004-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2004175740-A
titleOfInvention Method for producing α-substituted norbornanyl acrylates
abstract A method for synthesizing a norbornene-based resist monomer suitable for production on an industrial scale is provided. An α-substituted acrylic acid is reacted directly with a substituted norbornene. The reaction is preferably performed in the presence of an acid catalyst. Examples of the acid catalyst include phosphoric acid, sulfuric acid, hydrochloric acid, p-toluenesulfonic acid, trifluoroacetic acid, trifluoromethanesulfonic acid, boron trifluoride, titanium tetrachloride, At least one selected from the group of tin chloride is preferred. According to the present invention, the reaction mixture is maintained at a low viscosity throughout the reaction and purification steps, so that handling thereof is significantly facilitated. [Selection diagram] None
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type http://data.epo.org/linked-data/def/patent/Publication

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