SU620491A1 - Method of obtaining oxides of dialkyl-4-oxyphenylphosphines - Google Patents

Method of obtaining oxides of dialkyl-4-oxyphenylphosphines

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Publication number
SU620491A1
SU620491A1 SU762389598A SU2380598A SU620491A1 SU 620491 A1 SU620491 A1 SU 620491A1 SU 762389598 A SU762389598 A SU 762389598A SU 2380598 A SU2380598 A SU 2380598A SU 620491 A1 SU620491 A1 SU 620491A1
Authority
SU
USSR - Soviet Union
Prior art keywords
dialkyl
oxyphenylphosphines
oxides
obtaining oxides
obtaining
Prior art date
Application number
SU762389598A
Other languages
Russian (ru)
Inventor
Вячеслав Васильевич Кормачев
Клара Васильевна Солодова
Татьяна Васильевна Васильева
Original Assignee
Чувашский государственный университет им. И.Н.Ульянова
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.)
Filing date
Publication date
Application filed by Чувашский государственный университет им. И.Н.Ульянова filed Critical Чувашский государственный университет им. И.Н.Ульянова
Priority to SU762389598A priority Critical patent/SU620491A1/en
Application granted granted Critical
Publication of SU620491A1 publication Critical patent/SU620491A1/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Изобретение относитс  к области химии фосфорорганических соединений с Р-С св зью, а именно к новому способу получени  окисей  иалкип-4-оксифенипфосфинов обшей формулыThis invention relates to the field of chemistry of organophosphorus compounds with a P – C bond, namely, to a new method for producing oxides of alipat-4-hydroxypheniphosphine general formulas

2j-S«4-0.2j-S "4-0.

где R - атсил,where R is atsil,

которые могут найти применение в качестве полупродуктов дл  получени  термо-, огнестойких красителей, комплексообразователей , биологически активных соединений, или огне-, термостойких фосфорилированных фенолформапьдегидных смол.which can be used as intermediates for the preparation of thermo-, fire-resistant dyes, complexing agents, biologically active compounds, or fire-, heat-resistant phosphorylated phenol-formahyde resins.

Известен способ получени  окиси дифенип-4-оксифенига|)осфина обработкой 57%-.ной йодистоводородной кислотой окиси дифенип-4-метоксифенилфосфина при нагревании до 150 С в присутствии фосфсфистой кислоты ij.A known method for producing diphenip-4-hydroxyphenig oxide) osphine by treating with 57% -. Hydroiodic acid of diphenip-4-methoxyphenylphosphine oxide when heated to 150 ° C in the presence of a phosphoric acid ij.

Наиболее близким к описываемому изобретению по технической сущности и достигаемому результату  вл етс  спсThe closest to the described invention to the technical essence and the achieved result is ATP

соб получени  окисей диалкил-, например диметил-4-оксифенипфосфинов, который заключаетс  в том, что диалки1Ь-4- -метоксифенилфосфин обрабатывают 48%- ной бромистоводородной кислотой при нагревании до 150-160 С в атмосфере аргона с последующим окислением полученного диалкид-4-оксифенипфосфина перекисью водородаJ2j. Выход конечного продукта составл ет 54% от теоретического .by preparing dialkyl- oxides, for example, dimethyl-4-hydroxypheniphosphines, which means that dialkyl-4-methoxyphenylphosphine is treated with 48% hydrobromic acid when heated to 150-160 ° C under argon atmosphere, followed by oxidation of the resulting dialkide-4- hydroxypheniphosphine hydrogen peroxide J2j. The yield of the final product is 54% of the theoretical.

.Недостатки этого способа - многостадийность процесса, необходимость использовани  большого избытка бромистоводородной кислоты, что приводит к значительному осмолению и затрудн ет выделение продуктов из реакционной массы , а также невысокий выход продукте.The disadvantages of this method are the multistage process, the need to use a large excess of hydrobromic acid, which leads to significant tarring and makes it difficult to isolate products from the reaction mass, as well as to a low yield.

Цель изобретени  - упрощение процесса и повышение выхода продуктов.The purpose of the invention is to simplify the process and increase the yield of products.

Это достигаетс  согласно описываемому способу получени  окисей диалхип-4-оксифенилфосфинов , который заключав с  в том, что окиси диалкип-4-хлорфенипThis is achieved according to the described method for producing dialip-4-hydroxyphenylphosphines, which concluded that dialkip-4-chlorophenip oxides

SU762389598A 1976-07-06 1976-07-06 Method of obtaining oxides of dialkyl-4-oxyphenylphosphines SU620491A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU762389598A SU620491A1 (en) 1976-07-06 1976-07-06 Method of obtaining oxides of dialkyl-4-oxyphenylphosphines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU762389598A SU620491A1 (en) 1976-07-06 1976-07-06 Method of obtaining oxides of dialkyl-4-oxyphenylphosphines

Publications (1)

Publication Number Publication Date
SU620491A1 true SU620491A1 (en) 1978-08-25

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Family Applications (1)

Application Number Title Priority Date Filing Date
SU762389598A SU620491A1 (en) 1976-07-06 1976-07-06 Method of obtaining oxides of dialkyl-4-oxyphenylphosphines

Country Status (1)

Country Link
SU (1) SU620491A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6733698B2 (en) * 2001-02-15 2004-05-11 Pabu Services, Inc. Mixture of mono-, bis- and tris-(hydroxyaryl) phosphine oxides useful to make polyglycidyl ethers or in epoxy compositions
US6887950B2 (en) 2001-02-15 2005-05-03 Pabu Services, Inc. Phosphine oxide hydroxyaryl mixtures with novolac resins for co-curing epoxy resins

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6733698B2 (en) * 2001-02-15 2004-05-11 Pabu Services, Inc. Mixture of mono-, bis- and tris-(hydroxyaryl) phosphine oxides useful to make polyglycidyl ethers or in epoxy compositions
US6887950B2 (en) 2001-02-15 2005-05-03 Pabu Services, Inc. Phosphine oxide hydroxyaryl mixtures with novolac resins for co-curing epoxy resins
US6955851B2 (en) 2001-02-15 2005-10-18 Pabu Services, Inc. Hydroxyaryl phosphine oxides, glycidyl ethers and epoxy compositions, composites and laminates derived therefrom
US7202311B2 (en) 2001-02-15 2007-04-10 Great Lakes Corporation Phosphine oxide hydroxyarl mixtures with novolac resins for co-curing epoxy resins
US7201957B2 (en) 2001-02-15 2007-04-10 Great Lakes Corporation Phosphine oxide hydroxyaryl mixtures with novolac resins for co-curing epoxy resins

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