http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1138238-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_94ff2d78578d95d1e8d3a2233c76188d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C11D3-361
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-386
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C02F5-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C11D3-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C02F5-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-38
filingDate 1966-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1968-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1138238-A
titleOfInvention Process for preparing hydroxydiphosphonic acids from elemental phosphorus and carboxylic acids
abstract 1,138,238. Hydroxydiphosphonic acids. PROCTER & GAMBLE CO. 29 July, 1966 [29 July, 1965; 31 May, 1966], No. 34223/66. Heading C2C. Hydroxydiphosphonic acids are prepared by (a) dispersing yellow or white phosphorus in an organic medium containing or consisting of a carboxylic acid, (b) introducing an oxidizing gas into the dispersion with vigorous mixing to form in situ an acid anhydride of trivalent phosphorus which then reacts with the carboxylic acid to form phosphite intermediates, (c) maintaining the reaction mixture at 70-170‹ C. either during or subsequent to the oxidizing step (b) or both to convert the phosphite intermediates to compounds containing P-C bonds and (d) hydrolysing the mixture with water to form a hydroxydiphosphonic acid. The carboxylic acid can suitably be an aliphatic mono- or poly-carboxylic acid having 2-30 carbon atoms, acetic acid being especially preferred. The acids may also be hydroxy or other substituted acids, e.g. phenylacetic acid or hydroxyacetic acid, and may be saturated, unsaturated, straight chain or branch chain. Mixtures of the above classes of acids may also be used. The preferred proportion of acid to phosphorus is 2-25 carboxylic groups per mole of phosphorus (P 4 ). The phosphorus should be dispersed in a finely divided state in the organic medium, optionally with heating, to give a particle diameter of preferably less than 2 cm., the term " dispersion " being defined as including any suspensions of finely divided solid or liquid particles in a liquid medium, the particles being of colloidal dimensions or larger, and molecular dispersions. The oxidizing gas may be oxygen and/or ozone, or air and may be added stepwise or incrementally, preferably at 20-140‹ C. The oxidizing step may be carried out in a stirred tank or a series of stirred tanks or with the oxidant gas flowing countercurrent to the dispersion in an agitated column. The phosphorus and acid may be reacted in the presence of a diluent such as excess acid, (C 3 H 7 ) 2 SO 2 , sulpholane, tetrachloroethane, (C 4 H 9 ) 2 O and diglyme. The free acid product may be neutralized with a base, e.g. NaOH or KOH, to form the corresponding salt. The hydrolysis step is suitably carried out at 90-170‹ C. When the carboxylic acids are solid at room temperature, a solvent may be used such as hydrocarbons, ethers and halogenated hydrocarbons such as CCl 4 , CS 2 and chlorobenzene. The solvent may also be selected from the diluents mentioned above.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9777027-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016534077-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015059287-A1
priorityDate 1965-07-29-04:00^^<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/substance/SID419521617
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559532
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416129933
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409060395
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419517214
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24404
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19095100
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523755
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID31347
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410697574
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419486645
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457773519
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419576106
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7964
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411295908
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14798
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14797
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID123286
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID757
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID107908
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8150
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559478
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524391
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407364031
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6591
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID999
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID977
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID176
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523291
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1549559
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419546960
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406903350
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24823

Total number of triples: 54.