http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1489695-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bb0a7b16a31bf7bc8b903ed8b717aab6
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03C8-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C8-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C8-10
filingDate 1975-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1977-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1489695-A
titleOfInvention Photographic dye diffusion transfer process
abstract 1489695 Dialkoxy benzene derivatives AGFAGEVAERT AG 10 Feb 1975 [12 Feb 1974] 5475/75 Heading C2C [Also in Divisions G2 and C4] 2 - Acetamido - 5 - hexadecylsulphonamido. 1,4 - dimethoxybenzene is prepared by adding hexadecylsulphochloride at room temperature to 2 - acetamido - 5 - amino - 1,4 - dimethoxybenzene in anhydrous pyridine, diluting with a little water, pouring on to ice and acidifying with concentrated HCl. 2-Amino-5-hexadecylsulphonamido - 1,4 - dimethoxybenzene is prepared by refluxing the above product with concentrated hydrochloric acid in ethanol and cooling. 2 - Nitro - 1,4 - didodecyloxybenzene is prepared by adding dropwise nitric acid of density 1À39 at room temperature to hydroquinone didodecyl ether in glacial acetic acid. 2 - Amino - 1,4 - didodecyloxybenzene is prepared by catalytically hydrogenating the above nitro compound in tetrahydrofuran in the presence of nickel at 30-35‹ C./50 atmospheres pressure. 2 - Acetamido - 1,4 - didodecyloxybenzene is prepared by adding acetic anhydride to the filtered hydrogenation solution above and precipitating with 1-2 times the volume of acetonitrile. 5 - Nitro - 2 - acetamido - 1,4- didodecyloxybenzene is prepared by suspending the last compound in glacial acetic acid, adding dropwise nitric acid of density 1À39 at room temperature and adding further glacial acetic acid. 5 - Nitro - 2 - amino - 1,4 - didodecyloxybenzene is prepared by refluxing the last compound with concentrated HCl in ethanol, adding strong NaOH solution till alkaline and precipitating with plenty of water. 2,5-Diamino- 1,4 - didodecyloxybenzene is prepared by catalytically hydrogenating the last compound.
priorityDate 1974-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID176
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409060395
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422782391
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559502
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422782392
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20311079
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422782393
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8028
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID154161004
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419521384
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20311081
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419547992
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1049
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558780
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419974635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12143638
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559283
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7918
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID314305
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419557048
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412550040
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20311075
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9016
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20311076
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559357
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20311077
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422782394
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426789629
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415935800
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID935
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422782395
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20311078
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422782396
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432085419
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406903350
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID944
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17995873
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14798
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6342

Total number of triples: 55.