http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0249556-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C68-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-96
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C68-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-96
filingDate 1987-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc46491cec22b9b223ce3c3d1399dd10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_442286d5d02331f898bc8b32e24879ca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e2f629360df184fb83580249e91b39d
publicationDate 1987-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0249556-A1
titleOfInvention Process for the preparation of alpha-halogenated organic esters of carbonic acid
abstract The invention relates to a process for the preparation of alpha-halogenated carbonates of formula characterized in that a particular aldehyde of formula R¹CHO is reacted in which R¹ represents a hydrogen atom, a substituted or unsubstituted radical, Cip to C en aliphatic, C₃ to C₂₀ cycloaliphatic, C₇ to C₁₅ araliphatic or C₆ to C₁₄ aromatic, with a particular haloformate of formula R² in which n is equal to 1 or 2 and R² represents a substituted or unsubstituted radical, C₂ to C en aliphatic and unsaturated, C₆ to C₁₄ aromatic, C₁ to C₂₀ aliphatic and monohalogenated in position 1, a succinimido group or a trihalo group -2,2,2 ethyl, when X represents a fluorine, chlorine, bromine or iodine atom, or R² represents an aliphatic radical in C₁ to C₂₀, substituted or not substituted when X represents a fluorine atom, in the presence of a catalyst chosen from aromatic tertiary amines, heteroaromatic amines, pyridines, pentaalkylsubstituted guanidines, tertiary phosphines, ammonium or quaternary phosphonium halides, alkali halides associated with a cation complexing agent and tetrasubstituted ureas, at a temperature between 50 ° and 100 ° C.n n n This new process makes it possible to simply obtain numerous alpha-halogenated carbonates very useful in the pharmaceutical and phytosanitary fields.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2602241-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2014342221-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0895991-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6458990-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0895991-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6632949-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013083418-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9969673-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2824096-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103987691-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015004195-A1
priorityDate 1986-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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