SU410029A1 - - Google Patents

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Publication number
SU410029A1
SU410029A1 SU1772072A SU1772072A SU410029A1 SU 410029 A1 SU410029 A1 SU 410029A1 SU 1772072 A SU1772072 A SU 1772072A SU 1772072 A SU1772072 A SU 1772072A SU 410029 A1 SU410029 A1 SU 410029A1
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SU
USSR - Soviet Union
Prior art keywords
heating
carried out
argon
vinyl phosphonate
phosphonito
Prior art date
Application number
SU1772072A
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Russian (ru)
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
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Priority to SU1772072A priority Critical patent/SU410029A1/ru
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Publication of SU410029A1 publication Critical patent/SU410029A1/ru

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Description

1one

Изобретение относитс  к новому ранее не известных типов фосфороргаиических соединений общей формулыThis invention relates to a new, previously unknown type of phosphorus compounds of the general formula

(RO).P (О) СН - СН,Р (О) (OR),(RO) .P (O) CH - CH, P (O) (OR),

Р (OR).P (OR).

где R - одинаковые или разные алкилы.where R is the same or different alkyls.

Полученные соединени  могут найти применение в качестве комплексообразователей, а также дл  синтеза новых типов фосфорорганических комплексонов и экстрагентов.The compounds obtained can be used as complexing agents, as well as for the synthesis of new types of organophosphorus complexones and extractants.

Предлагаемый способ получени  алкилен (фосфонито)дифосфопатов заключаетс  в том, что тетраалкилпирофосфит подвергают взаимодействию с диалкилвинилфосфонатом при нагревании, желательно до 100-200°С, в атмосфере инертного газа, например аргона, с последующим выделением целевого продукта известными нриемами.The proposed method for the preparation of alkylene (phosphonito) diphosphopates consists in that the tetraalkylpyrophosphite is reacted with the dialkyl vinyl phosphonate by heating, preferably to 100-200 ° C, in an inert gas atmosphere, such as argon, followed by isolation of the target product by known methods.

Процесс протекает по схеме:The process proceeds according to the scheme:

(RO).P-O-P (OR). + (R0),p (О) СН сн.(RO) .P-O-P (OR). + (R0), p (O) CH.

(RO),P (О) СН - СН,Р (О) (OR), (RO), P (O) CH - CH, P (O) (OR),

Р (OR),P (OR),

где R - одинаковые или разные алкилы.where R is the same or different alkyls.

Пример. Получение тетраэтнлэтилен (О,0диэтилфосфонито ) -1,2-дифосфоната (реакцию провод т в токе сухого аргона).Example. Preparation of tetraethylethylene (O, 0-diethylphosphonite) -1,2-diphosphonate (the reaction is carried out in a stream of dry argon).

Смесь 13 г (0,05 моль) тетраэтилпирофосфита и 8,2 г (0,05 моль) диэтилвинилфосфоната нагревают 3 час при 170°С. Контроль за ходом реакции ведут методом ИК-спектроскопии . При исчезновении полосы поглощени , соответствующей С С-св зи винилфосфоната , нагревание прекращают. Реакционную смесь перегон ют в вакууме. Получают 15 г (70%) целевого продукта, т. кип. 140°С/A mixture of 13 g (0.05 mol) of tetraethyl pyrophosphite and 8.2 g (0.05 mol) of diethyl vinyl phosphonate is heated for 3 hours at 170 ° C. Monitoring the progress of the reaction is carried out by IR spectroscopy. With the disappearance of the absorption band corresponding to the C – C bond of the vinylphosphonate, heating is stopped. The reaction mixture is distilled in vacuo. Obtain 15 g (70%) of the desired product, t. Kip. 140 ° C /

/0,01 мм рт. ст. df I,l362, no/ 0.01 mm Hg. Art. df I, l362, no

1,4542. С 40,14; П 7,62; Р 21,57. MRo1.4542. C 40.14; P 7.62; R 21.57. Mro

Найдено, 100,7.Found 100.7.

СиНззОаРз. SyNzOOrz.

С 39,83; Н 7,88; Р 22,01. Вычислено, %: MRn 100,9.C 39.83; H 7.88; P 22.01. Calculated,%: MRn 100.9.

Предмет изобретени Subject invention

Claims (2)

1.Способ получени  алкилен(фосфонито)дифосфонатов , отличающийс  тем, что тетраалкилпирофосфит подвергают взаимодействию с диалкилвинилфосфонатом в атмосфере инертного газа, например аргона, при нагревании с последующим выделением целевого продукта известными методами.1. A method for producing alkylene (phosphonito) diphosphonates, characterized in that the tetraalkyl pyrophosphate is reacted with a dialkyl vinyl phosphonate under an inert gas such as argon, with heating, followed by isolation of the target product by known methods. 2.Способ по п. 1, отличающийс  тем, что процесс ведут при 100-200°С.2. A method according to claim 1, characterized in that the process is carried out at 100-200 ° C.
SU1772072A 1972-04-13 1972-04-13 SU410029A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1772072A SU410029A1 (en) 1972-04-13 1972-04-13

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1772072A SU410029A1 (en) 1972-04-13 1972-04-13

Publications (1)

Publication Number Publication Date
SU410029A1 true SU410029A1 (en) 1974-01-05

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SU (1) SU410029A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0023173A1 (en) * 1979-07-09 1981-01-28 Societe Nationale Elf Aquitaine (Production) Diphosphonic and triphosphonic acid esters, their preparation and applications
US4460548A (en) * 1979-07-09 1984-07-17 Societe Nationale Elf Aquitaine (Production) Extraction of uranium with diphosphonic compounds
US4464346A (en) * 1979-07-09 1984-08-07 Societe Nationale Elf Aquitaine (Production) Extraction of uranium with triphosphonic esters
US4587034A (en) * 1979-07-09 1986-05-06 Societe Nationale Elf Aquitaine (Production) Triphosphonic esters
US4631142A (en) * 1979-07-09 1986-12-23 Societe Nationale Elf Aquitaine (Production) Diphosphonic extractants

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0023173A1 (en) * 1979-07-09 1981-01-28 Societe Nationale Elf Aquitaine (Production) Diphosphonic and triphosphonic acid esters, their preparation and applications
US4460548A (en) * 1979-07-09 1984-07-17 Societe Nationale Elf Aquitaine (Production) Extraction of uranium with diphosphonic compounds
US4464346A (en) * 1979-07-09 1984-08-07 Societe Nationale Elf Aquitaine (Production) Extraction of uranium with triphosphonic esters
US4587034A (en) * 1979-07-09 1986-05-06 Societe Nationale Elf Aquitaine (Production) Triphosphonic esters
US4631142A (en) * 1979-07-09 1986-12-23 Societe Nationale Elf Aquitaine (Production) Diphosphonic extractants

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