SU410029A1 - - Google Patents
Info
- 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
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- heating
- carried out
- argon
- vinyl phosphonate
- phosphonito
- Prior art date
Links
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)
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 |
Family
ID=20510430
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1772072A SU410029A1 (en) | 1972-04-13 | 1972-04-13 |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU410029A1 (en) |
Cited By (5)
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 |
-
1972
- 1972-04-13 SU SU1772072A patent/SU410029A1/ru active
Cited By (5)
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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