SU196821A1 - Method of producing vinyl esters of 0,0-dialkyl-o-oxyalkylphosphate - Google Patents
Method of producing vinyl esters of 0,0-dialkyl-o-oxyalkylphosphateInfo
- Publication number
- SU196821A1 SU196821A1 SU1079730A SU1079730A SU196821A1 SU 196821 A1 SU196821 A1 SU 196821A1 SU 1079730 A SU1079730 A SU 1079730A SU 1079730 A SU1079730 A SU 1079730A SU 196821 A1 SU196821 A1 SU 196821A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dialkyl
- vinyl esters
- oxyalkylphosphate
- producing vinyl
- sulfur
- Prior art date
Links
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 title description 4
- 229920001567 Vinyl ester Polymers 0.000 title description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- 239000011593 sulfur Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- -1 ethoxyethylthiophosphate Chemical compound 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 230000002194 synthesizing Effects 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000015450 Tilia cordata Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 210000003462 Veins Anatomy 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
Description
Предлагают способ получени виниловых зфиров 0,0-дналкил-О-оксиалкилтиофосфатов, состо щий в том, что диалкилфинилоксиалкилфосфат подвергают взанмодейств 1Ю с серой с последующим выделением целевого продукта известпым способом.A method is proposed for the preparation of the vinyl esters of 0,0-dinalkyl-O-hydroxyalkyl thiophosphates, in which the dialkyl-phenyloxyalkyl phosphate is exposed to sulfur with sulfur followed by isolation of the desired product by the lime method.
Пример 1. Синтез О.О-диэтил-О-винилоксиэтилтиофосфата . К 8,0 г диэтилвипилоксиэтилфосфита прибавл ют 1,2 г порошковой серы. Происходгг экзотермическа реакци , в результате которой темнература поднимаетс до 120°С, а сера полностью раствор етс . Полученный прозрачный слегка желтоватый продукт достаточно чист дл осуидествлепи превращений по винильной группе. Дл целей полимеризации продукт очищают перегонкой . Получают 9,1 г (выход 99,б5/о от теоретического ) 0,0-диэтил-О-вииилоксиэтилтиофосфата; т. кип. 80°С, по 1,4667; df 1,1097; MRo 60,04; MRo 60,42.Example 1. Synthesis of OO-diethyl-O-vinyloxyethyl thiophosphate. To 8.0 g of diethylvipyloxyethylphosphite was added 1.2 g of powdered sulfur. The exothermic reaction takes place, as a result of which the temneture rises to 120 ° C and the sulfur completely dissolves. The resulting clear, slightly yellowish product is sufficiently pure to transform into the vinyl group. For polymerization purposes, the product is purified by distillation. 9.1 g are obtained (yield 99, b5 / o from the theoretical) 0,0-diethyl-O-viiiyloxyethyl thiophosphate; m.p. 80 ° C, 1.4667 each; df 1.1097; MRo 60.04; MRo 60.42.
найд.выч.found
Найдено, %: С 39,98; Н 7,13; Р 12,40; S 13,28. CgHnOiSP.Found,%: C 39.98; H 7.13; P 12.40; S 13.28. CgHnOiSP.
Вычислено, о/„: С 39,99; Р-1 7,13; Р 12,89; S 13,31.Calculated, о / „: С 39.99; P-1 7.13; R 12.89; S 13.31.
Пример 2. Синтез 0,0-диэтнл-О-випилокс этоксиэтнлтиофосфата . 2,0 г диэтилвинилокснэтокснэти/1фосф1гга смешивают с 0,25 г порошковой серы. После окончани экзотермичной реакции и растворени всей серы продукт перегон ют, получают 2,23 г вен1ества;Example 2. Synthesis of 0,0-diethyl-O-vipilox ethoxyethylthiophosphate. 2.0 g of diethylvinyloxnatoxneti / 1phosph1gga is mixed with 0.25 g of powdered sulfur. After the termination of the exothermic reaction and the dissolution of all sulfur, the product is distilled; 2.23 g of vein is obtained;
2020
2020
1I2 -113°C; 1I2 -113 ° C;
1,4672; 1.4672;
1,1181;1.1181;
ПоBy
т. КПП.t. CAT.
MRo „ 70,89; MRo 71,50.MRo 70.89; MRo 71.50.
и а ид.and a go
вычCalc
С 42,34;C 42.34;
Пайдеио, Paideio,
Н 7,44H 7.44
Р 10,69; S 11,14.R 10.69; S 11.14.
CioH iOjSP.CioH iOjSP.
Вычислено, Calculated
%: С 42,24; П 7,44; Р 10,89; S 11,27.%: C, 42.24; P 7.44; R 10.89; S 11.27.
Предмет изобретени Subject invention
Способ получени виниловых эфнров 0,0диалкил-0-оксиалкнлтиофосфатов , отличаю1цийс тем, что дналкилвинилоксналкилфосфат подвергают взаимодействию с серой с последующим выделением целевого продукта известным снособом.The method of producing vinyl esters of 0.0 dialkyl-0-hydroxyalkyl thiophosphates, is distinguished by the fact that the alkyl vinyloxy xyl alkyl phosphate is reacted with sulfur, followed by isolation of the target product by a known method.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU196821A1 true SU196821A1 (en) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU196821A1 (en) | Method of producing vinyl esters of 0,0-dialkyl-o-oxyalkylphosphate | |
| BG63542B1 (en) | Methods and intermediate compounds for producing substituted chromanol derivatives | |
| EP0009306B1 (en) | Anti-arthritic hydroxyacetic acid derivatives, pharmaceutical compositions thereof, and processes for their manufacture | |
| US2630452A (en) | Beta-mercaptopropionitrile and processes for their preparation | |
| SU259877A1 (en) | METHOD OF GETTING DIALKYL-8- [a-ALKOXI ( | |
| SU218140A1 (en) | METHOD OF OBTAINING ETHYL-p-NAFTIL-p, p-DICHLOROVINYL-PHOSPHATE | |
| SU273200A1 (en) | METHOD FOR OBTAINING N-ACYL-S- (O, 0-DIALKYLTIOPHOSPHORYL) -CYSTEIN ETHERS | |
| SU256764A1 (en) | METHOD OF OBTAINING N-PHOSPHOLYLATED CYCLIC URETHANES | |
| SU248679A1 (en) | ||
| SU152594A1 (en) | ||
| SU305655A1 (en) | ||
| SU289094A1 (en) | Method of producing derivatives a-phenylvinylphosphate | |
| SU329160A1 (en) | Method of producing asymmetric 1,1-diaryl, iclopentene | |
| SU183752A1 (en) | B. Ya. L. P. V. Vershinin and L. I. Beim "^^^;: ^ -. P.,: ,, fii'fi '^; ::. V -'-; / | |
| SU386963A1 (en) | ALL-UNION mpt ^ pt'pf:! - H :: v4riO "EKA | |
| SU351867A1 (en) | METHOD OF OBTAINING OLIGOMERIC BIS (CYCLOPENTADIENYL) COMPOUNDS | |
| SU245133A1 (en) | WAY OF OBTAINING VINYL ETHER p- (FURIL-2) ACRYLIC ACID | |
| SU468911A1 (en) | The method of obtaining -diethylamide tert.-butylperoxymethyl esters of dicarbamic acids | |
| SU245801A1 (en) | Method of producing 6-cycloalkyl substituted dihydro-pyrone | |
| SU281466A1 (en) | Method of producing esters of N-acyl-S- (O, O-dialkylphosphoryl) -cysteine | |
| SU316689A1 (en) | METHOD OF OBTAINING | |
| SU172304A1 (en) | Method for producing phenyl ethers of perfluorocarbonic acids | |
| SU341798A1 (en) | Method of producing non-symmetric diaminoalkylsulfides of the pyridine series | |
| SU239956A1 (en) | METHOD FOR OBTAINING p- (Aryloxy-acyl) -Hydrazides of 4-AMINO-3,5,6-TRICHLORPICOLINIC ACID | |
| SU237150A1 (en) | METHOD OF OBTAINING DERIVATIVE S-ACETYLEDITIOPHOSPHATE |