http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1189531-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C257-22
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C257-22
filingDate 1982-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1985-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef4cbb1c8ab3e78ab5d7804206d4be4b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_860b2e0250f96bdc759ec85b74a9ba5a
publicationDate 1985-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1189531-A
titleOfInvention Process for the preparation of hydrazidines
abstract ABSTRACT PREPARATION OF HYDRAZIDINES A new one-step process for the preparation of hydrazidines of the general formula (I), in which R represents an optionally substituted alkyl group, an optionally substituted cycloalkyl group, an optionally sub-stituted aryl group or an optionally substituted aralkyl group, or their acid addition salts, in high yield comprises reacting iminoalkyl ethers of the general formula (II), in which R has the abovementioned meaning and R1 represents an optionally substituted alkyl group or an optionally substituted cycloalkyl group, or their acid addition salts, with hydrazine in solvents under reduced pressure and at temperatures between -80 and +100°C, the reaction being effected in the presence of water present in the solvent and/or in the hydrazine by employing it as hydrazine hydrate. The hydrazidines of formula (I) and their salts are valuable intermediates in heterocyclic chemistry, for example for the synthesis of herbicidally active as-triazinones.
priorityDate 1981-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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