http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-679854-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-295
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-295
filingDate 1949-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a8f18e48adb74df8d40cb6644b05613
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b6a6b8c2df1ab94a117d04545eedd0e
publicationDate 1952-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-679854-A
titleOfInvention Manufacture of pimelic acid
abstract Pimelic acid is made by contacting at a pressure high enough to maintain the reactants in the liquid phase delta3-tetrahydrobenzaldehyde or its trimer or an alkaline condensation product of the monomer such as is obtained on treatment with an aqueous alkali at low temperatures, with an aqueous solution of an alkali metal hydroxide, the reaction mixture being brought to a temperature within the range 250-400 DEG C., and the acid thereafter separated. Under more severe reaction conditions, e.g. above about 300 DEG C., only a small quantity of the corresponding alicyclic alcohol is formed. The hydroxides, e.g. those of sodium and potassium alone or mixed, are preferably used in excess, e.g. a 10-80 per cent excess of theory is specified. Preferably, the concentration of the hydroxide is about 30-40 per cent by weight. Pressures should be sufficient to ensure a liquid phase reaction. A mixture of the above monomer and trimer may be used, e.g. the product obtained by acid trimerization, and the trimer may be in solution in an inert solvent. In examples, the monomer is treated in an autoclave in (1), (5) and (6) with aqueous sodium hydroxide at temperatures ranging from 260 DEG to 360 DEG C. and at pressures up to 190 atmos. gauge and in (4) with aqueous potassium hydroxide at 300 DEG C. under pressure and in (2) the trimer, and in (3) a mixture of the monomer and trimer, are autoclaved with aqueous sodium hydroxide at 340-360 DEG C. under pressure, and in all cases pimelic acid is separated after reaction times varying from 3 to 24 hours.
priorityDate 1949-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 26.