<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/RXNO?iri=http://purl.obolibrary.org/obo/RXNO_0000165"?>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RXNO_0000165 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/RXNO_0000165">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Schotten-Baumann reaction</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/RXNO_0000331"/>
        <oboInOwl:hasOBONamespace rdf:datatype="http://www.w3.org/2001/XMLSchema#string">RXNO</oboInOwl:hasOBONamespace>
        <oboInOwl:id rdf:datatype="http://www.w3.org/2001/XMLSchema#string">RXNO:0000165</oboInOwl:id>
        <ns3:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">The coupling of an alcohol or amine with an acyl chloride to give an ester or amide. A two-phase solvent system is often used, to enable the acid generated during the reaction to be neutralised by the aqueous base, while the starting materials and products remain in the organic phase.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">https://www.rsc.org/Merck-Index/reaction/r392/</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/RXNO_0000331 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/RXNO_0000331">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">substitution step</rdfs:label>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



