CAS: 1498-51-7; Ethyl Phosphorodichloridate

相似化合物

1455-05-6 677-24-7 4167-02-6

上下游产品

CAS号64-17-5 乙醇 | CAS号20195-06-6 PHORATE-OXON | CAS号2511-10-6 O,S-二乙基甲基硫代磷酸 | CAS号32345-29-2 增效磷 | CAS号10428-96-3 S-allyl-O,O-die... | CAS号40626-35-5 速杀硫磷 | CAS号3167-63-3 氯甲基膦酸二乙酯 | CAS号121044-50-6 (E)-diethyl-3-c... | CAS号10419-78-0 (1-Chloroethyl)... | CAS号10448-50-7 Triphosphoric a... | CAS号32634-95-0 6-亚甲基孕甾-4-烯-17A... | CAS号814-49-3 氯磷酸二乙酯 | CAS号75-00-3 氯乙烷 | CAS号10025-87-3 三氯氧磷 | CAS号2510-93-2 N-[chloro(ethox... | CAS号24590-37-2 N-[chloro(ethox... | CAS号2404-65-1 N-[dimethylamin... | CAS号18368-64-4 2-氯-5-甲基吡啶 | CAS号1007-80-3 1,3,2-Dioxaphos...

乙醇置于三氯氧磷体系中,用75%的收率获得二氯磷酸乙酯
参考文献:合成von Phosphorsäure烷基酯二酰胺
标题:合成von Phosphorsäure烷基酯二酰胺
摘要:在 Vorangegangenen 手套.Beschrieben Wir Verfahren Zur Darstellung Von Phosphorsäure-Phenylester-Und Phosphorsäure-4-Nitro-Phenylester-N,N'-Diamiden.In Der Vorliegenden Veröffentlichung Wird Die Synthese Von Phosphorsäurealkylester-N,N'-Diamiden Aus Phosphorsäurealkylesterdichloride Und Primären Aminen Geschildert.
Doi:10.1002/ardp.19823150703

专利信息

专利号:US-10111867-B2
优先权日:2015-02-17
标题:Process and intermediates for the preparation of perampanel
发明人：MAROM EHUD; RUBNOV SHAI
权利人:MAPI PHARMA LTD
摘要:The present invention describes a process for the synthesis of 3-(2-cyanophenyl)-5-(2-pyridyl)-1-phenyl-1,2-di-hydro-pyridin-2-one (Perampanel) represented by the structure of formula (1), and salts thereof, especially salts with pharmaceutically acceptable acids. The present invention further relates to certain intermediates formed and/or used in such process.

专利号:WO-2007057690-A1
优先权日:2005-11-18
标题:Desymmetrisation process for the production of cyclic phosphines used as ligands in enantioselective synthesis catalysts
发明人：GOUVERNEUR VERONIQUE
权利人:ISIS INNOVATION; GOUVERNEUR VERONIQUE
摘要:The present invention relates to a process for producing P-chiral cyclic phosphines, to a process for producing P-prochiral phosphine derivatives, to a process for preparing the (E,E) geometric isomers of P-chiral phosphine derivatives, to the P-prochiral phosphine derivatives, to the P-chiral cyclic phosphine derivatives, to hydroxyalkylphenylphosphine derivatives, to catalysts comprising the P-chiral cyclic phosphine derivatives or the hydroxyalkylphenylphosphine derivatives, to catalysts comprising a metal and a ligand where the ligand is, is derivable from or is obtainable from the P-chiral cyclic phosphine derivatives or the hydroxyalkylphenylphosphine derivatives, to the use as a catalyst of the P-chiral cyclic phosphine derivatives or the hydroxyalkylphenylphosphine derivatives, to the use as a catalyst of a compound comprising a metal and a ligand where the ligand is, is derivable from or is obtainable from the P-chiral cyclic phosphine derivatives or the hydroxyalkylphenylphosphine derivatives, and to a process for synthesising an organic compound whereby the synthesis includes and enantioselective reaction catalysed by the above catalyst.

专利号:CA-2743700-C
优先权日:2008-12-15
标题 :Stereoselective synthesis of piperidine derivatives

专利号:JP-2012512172-A
优先权日:2008-12-15
标 题:Stereoselective synthesis of piperidine derivatives.

专利号:RU-2021277-C1
优先权日:1991-01-14
标 题:Method of synthesis of o-methyl- or o-ethyldichlorophosphates

专利号:US-7022842-B2
优先权日:2000-12-21
标 题:Process for synthesizing beta-lactam
发明人：HATAKEDA KIYOTAKA; SATO OSAMU; KANAKUBO MITSUHIRO; IKUSHIMA YUTAKA; TORII KAZUO
权利人:NAT INST OF ADVANCED IND SCIEN
摘要:It is an object of the present invention to provide a method for synthesizing β-lactams and a method for manufacturing β-lactams in water of high-temperature and under high-pressure, and the present invention relates to a β-lactam synthesis method which is characterized in that β-lactams are synthesized by reacting β-amino acids in water at high-temperature and under high-pressure, this method being further characterized in that β-lactams are synthesized at a high speed by cyclizing β-amino acids in water at high-temperature and under high-pressure in which the temperature range is 200° C. or higher and the pressure range is 10 MPa or greater, and the present invention also relates to a method for manufacturing β-lactams which is characterized in that β-lactams are synthesized by reacting β-amino acids in water at high-temperature and under high-pressure, and are then separated and purified using a column separation medium.