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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D339-08
filingDate 2004-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_037eac2779c87e9bf1742b753533f82d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe2a27e2f098ad6b6ec1c7a16ea5ad1a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72277488473b2cb40cc7fb40118ee5c1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_461398505e8bc4cde67f5d67dcf8a139
publicationDate 2006-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2006124338-A
titleOfInvention Method for producing 2,5-bis (aminomethyl) -1,4-dithiane compound
abstract Provided is a method for industrially advantageously and efficiently producing a 2,5-bis (aminomethyl) -1,4-dithiane compound useful as a raw material for producing optical products, particularly high refractive index plastic lenses. (A) A 2,5-bis (halomethyl) -1,4-dithiane compound (1), an aldehyde (3) and ammonia are reacted, and the remaining ammonia is distilled off from the obtained reaction solution. Then, an acid is added to the reaction solution and stirred, or (B) 2,5-bis (halomethyl) -1,4-dithiane compound (1), aldehyde (4) and ammonia are reacted, The resulting reaction solution is stirred in the presence of water while removing the aldehyde (4). (In the formula, R 1 represents an alkyl group having 1 to 6 carbon atoms, R 2 represents an alkyl group or a phenyl group, R 3 represents an alkyl group having 2 to 6 carbon atoms, and X represents a halogen atom.) ) [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009270010-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010037304-A
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type http://data.epo.org/linked-data/def/patent/Publication

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