http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104788419-A

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-30
filingDate 2014-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9341a115910ee30e2ad45863ba82cd8f
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publicationDate 2015-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104788419-A
titleOfInvention Chiral (2,2-dimethyl-1,3-dioxolan-4-yl) hydroxymethanesulfonate and its preparation method and application
abstract The invention provides a chiral (2,2-dimethyl-1,3-dioxolan-4-yl) hydroxymethanesulfonate and its preparation method and application, relating to fine organic chemical and pharmaceutical intermediates field. The preparation method of the chiral (2,2-dimethyl-1,3-dioxolan-4-yl) hydroxymethanesulfonate comprises: synthesizing chiral glyceraldehyde acetone; Dissolve acetone with ethanol, then add potassium metapyrodisulfate, lithium sulfite, lithium bisulfite, potassium bisulfite, calcium bisulfite or magnesium bisulfite and water, and stir at 20-50°C Filter after the reaction to obtain the initial product; the initial product is dried to obtain chiral (2,2-dimethyl-1,3 dioxolane-4-yl) hydroxy methanesulfonate; the chiral ( 2,2-Dimethyl-1,3-dioxolan-4-yl) hydroxymethanesulfonate can replace chiral glyceraldehyde acetone to participate in Wittig reaction.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108069933-A
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Total number of triples: 25.