PROCESS FOR THE PREPARATION OF PHOSPHORIC ESTERS AND THIO PHOSPHORIC ESTERS
Aryl or aliph. phosphate and thiophosphate esters were prepd. by treatment of a phenol with POCl3 or PSCl3 in the presence of an alkali metal carbonate or hydroxide, H2O, and an org. solvent. Thus, 139.1 g 4-O2NC6H4OH in 2000 mL Me2CO were treated with 55.2 g POCl3, then immediately treated with 96....
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creator | YAMAMOTO RYUICHI TORISU MASAAKI |
description | Aryl or aliph. phosphate and thiophosphate esters were prepd. by treatment of a phenol with POCl3 or PSCl3 in the presence of an alkali metal carbonate or hydroxide, H2O, and an org. solvent. Thus, 139.1 g 4-O2NC6H4OH in 2000 mL Me2CO were treated with 55.2 g POCl3, then immediately treated with 96.0 g 45% NaOH over 10 min at |
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Thus, 139.1 g 4-O2NC6H4OH in 2000 mL Me2CO were treated with 55.2 g POCl3, then immediately treated with 96.0 g 45% NaOH over 10 min at <=30 C with rapid stirring, and the mixt. was kept 5 h to give 64% (4-O2NC6H4O)PO; similarly prepd. were 90% (4-O2NC6H4O)3PS, and 77% (BuCHEtCH2O)3PO.</description><language>eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1983</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19830312&DB=EPODOC&CC=KR&NR=830000552A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19830312&DB=EPODOC&CC=KR&NR=830000552A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>YAMAMOTO RYUICHI</creatorcontrib><creatorcontrib>TORISU MASAAKI</creatorcontrib><title>PROCESS FOR THE PREPARATION OF PHOSPHORIC ESTERS AND THIO PHOSPHORIC ESTERS</title><description>Aryl or aliph. phosphate and thiophosphate esters were prepd. by treatment of a phenol with POCl3 or PSCl3 in the presence of an alkali metal carbonate or hydroxide, H2O, and an org. solvent. Thus, 139.1 g 4-O2NC6H4OH in 2000 mL Me2CO were treated with 55.2 g POCl3, then immediately treated with 96.0 g 45% NaOH over 10 min at <=30 C with rapid stirring, and the mixt. was kept 5 h to give 64% (4-O2NC6H4O)PO; similarly prepd. were 90% (4-O2NC6H4O)3PS, and 77% (BuCHEtCH2O)3PO.</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1983</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZPAOCPJ3dg0OVnDzD1II8XBVCAhyDXAMcgzx9PdT8HdTCPDwDwbiIE9nBdfgENegYAVHPxegQk9_TCkeBta0xJziVF4ozc2g6OYa4uyhm1qQH59aXJCYnJqXWhLvHWRhbAAEpqZGjsbEqAEAqBkt6g</recordid><startdate>19830312</startdate><enddate>19830312</enddate><creator>YAMAMOTO RYUICHI</creator><creator>TORISU MASAAKI</creator><scope>EVB</scope></search><sort><creationdate>19830312</creationdate><title>PROCESS FOR THE PREPARATION OF PHOSPHORIC ESTERS AND THIO PHOSPHORIC ESTERS</title><author>YAMAMOTO RYUICHI ; TORISU MASAAKI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_KR830000552A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1983</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>YAMAMOTO RYUICHI</creatorcontrib><creatorcontrib>TORISU MASAAKI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>YAMAMOTO RYUICHI</au><au>TORISU MASAAKI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PROCESS FOR THE PREPARATION OF PHOSPHORIC ESTERS AND THIO PHOSPHORIC ESTERS</title><date>1983-03-12</date><risdate>1983</risdate><abstract>Aryl or aliph. phosphate and thiophosphate esters were prepd. by treatment of a phenol with POCl3 or PSCl3 in the presence of an alkali metal carbonate or hydroxide, H2O, and an org. solvent. Thus, 139.1 g 4-O2NC6H4OH in 2000 mL Me2CO were treated with 55.2 g POCl3, then immediately treated with 96.0 g 45% NaOH over 10 min at <=30 C with rapid stirring, and the mixt. was kept 5 h to give 64% (4-O2NC6H4O)PO; similarly prepd. were 90% (4-O2NC6H4O)3PS, and 77% (BuCHEtCH2O)3PO.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | PROCESS FOR THE PREPARATION OF PHOSPHORIC ESTERS AND THIO PHOSPHORIC ESTERS |
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