http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108558627-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2602-08
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-46
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-64
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-46
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-747
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-64
filingDate 2018-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108558627-B
titleOfInvention Method for preparing 5-hydroxy-1-indanone
abstract The invention provides a method for preparing 5-hydroxy-1-indanone, which comprises the following steps: dissolving anisole and 3-chloropropionyl chloride in dichloromethane to obtain a multi-component mixture AlCl 3 /LiCl、AlCl 3 /LiCl/NaCl、AlCl 3 LiCl/NaBr or AlCl 3 Reacting at room temperature for 8-15 hours under the catalysis of LiCl/NaI Lewis acid catalyst to prepare an intermediate 3-chloro-4' - (methoxyl) propiophenone, and evaporating dichloromethane; then heating to 100-170 ℃ melting state, continuing to react for 4-8 hours, cooling, pouring the reactant into ice water, adjusting the pH to 3-5 with hydrochloric acid, extracting with ethyl acetate, drying the organic phase, removing the solvent, and purifying to obtain the 5-hydroxy-1-indanone.
priorityDate 2018-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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