http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-1931286-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D339-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D339-06
filingDate 1969-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43e39273c26c71ef76814d603c12dc8d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_073f6752b6a4d01de89d0be811d7e0e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70275293ee0a9caf42e3d2164d0d9fbc
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publicationDate 1970-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-1931286-A1
titleOfInvention Process for the preparation of substituted methylenedithiolanes
abstract Methylene-2-dithiolanes 1,3 from alkene monothiocarbonates and thioamides. G5-. Have the C atom of the CH2 group outside the ring substituted by a hydrocarbon group. They are suitable as sulphurising agents and intermediates in the synthesis of heterocyclic cpds. with 2 S atoms. They are prepared, pref. at 100 - 250 degrees C, particularly 130 - 180 degrees C (150 - 170 degrees C). Pref. monothiocarbonates are derived from a mono-olefin (such as ethylene, propylene or a C4-8 ethylenic hydrocarbon) the chain of which also contains aryl or cycloalkyl groups. Pref. thioamides are alkyl or aryl thioacetamides, the latter being optionally substituted with C1-12 alkyl groups, Cl or Br atoms. In an example, 0.2 moles phenylthioacetamide and 0.2 moles ethylene monothiocarbonate are heated for 1 hr. at 160 degrees C. Benzylidene-2-dithiolane-1,3 is obtained in 67% yield.
priorityDate 1968-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 43.