http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-115074403-A

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filingDate 2022-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2022-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-115074403-A
titleOfInvention 4-(Methylhydroxyphosphoryl)-2-carbonylbutyric acid, the key intermediate of L-Glufosinate-ammonium
abstract The invention provides 4-(methylhydroxyphosphoryl)-2-carbonyl butyric acid, a key intermediate of L-glufosinate 2-(ethoxy-methylphosphoryl)-ethanol; in the carrier dispersed with copper oxide, feed oxygen to react to obtain 2-(ethoxy-methylphosphoryl)-acetaldehyde; 2-(ethoxy-methylphosphoryl)-acetaldehyde; base-methylphosphoryl)-acetaldehyde and glycine, add L-threonine acetalase, coenzyme pyridoxal phosphate, MnCl 2 , and react to obtain 4-(methylhydroxyphosphoryl)-threonine; 4 -(Methylhydroxyphosphoryl)-threonine and L-threonine deaminase react to obtain 4-(methylhydroxyphosphoryl)-2-carbonylbutyric acid through ultrafiltration. The two-step enzymatic method is adopted, no low-temperature cold source below 0°C is used, and the reaction conditions are mild. The enzymatic catalytic reaction is coupled with an ultrafiltration system, and the catalytic enzyme is recovered, and the yield is over 86%. 4-(methylhydroxyphosphoryl)-2-carbonylbutyric acid is a key intermediate in the synthesis of L-glufosinate-ammonium.
priorityDate 2022-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ5V3L1
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP29271
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7268
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419557752
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450926304
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Total number of triples: 438.