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SU58184A1 - The method of obtaining nitrosodimethylaniline - Google Patents

The method of obtaining nitrosodimethylaniline

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Publication number
SU58184A1
SU58184A1 SU29002A SU29002A SU58184A1 SU 58184 A1 SU58184 A1 SU 58184A1 SU 29002 A SU29002 A SU 29002A SU 29002 A SU29002 A SU 29002A SU 58184 A1 SU58184 A1 SU 58184A1
Authority
SU
USSR - Soviet Union
Prior art keywords
nitrosodimethylaniline
obtaining
solution
reaction
color
Prior art date
Application number
SU29002A
Other languages
Russian (ru)
Other versions
SU19439A1 (en
Inventor
Д.В. Розенгауз
Original Assignee
Д.В. Розенгауз
Filing date
Publication date
Application granted granted Critical
Publication of SU19439A1 publication Critical patent/SU19439A1/en
Application filed by Д.В. Розенгауз filed Critical Д.В. Розенгауз
Priority to SU29002A priority Critical patent/SU58184A1/en
Publication of SU58184A1 publication Critical patent/SU58184A1/en

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Description

могут быт1 крупными, но должны быть просе ны от пыли). При размешивании начинают процсс;- восстановлени . След т, чтобы все врем  была кисла  реакцн , дли чего придают част ми еще сол но кислоты . К концу восстановлени  реакци  должна быть не слишком кис,тон, чтобы ие образовать лишни.х количеств FeCl;. Всего дать :5i) ,o-ii кислоты не более 38и с на весь П1юцесс ннтрозировани  и иоостаноилени . Темнор.1тура раство| а к концу восстанов;1ени  может достигнуть 30 . По окончании Босстановлеии  раствор делаетс  прозрачным , имеет зеленоватый цвет и дает на конго слабо сиреневый вытек, а на фильтровальной бумаге - Слабо желтый вытек. вл ют сто ть сутки, в теченне которы.ч нрофи,1ьтрован11ы1| раствор де.шетс  сонершеино бесцветным, носле чего ею отфильт|ю ыва1от от чугунных стружек. Чугунные стружкн пром.1вают небольшим количеством воды и эту воду приливают к раствору н-аминодиметиланилина . аннлина нутем обработки сол нокислого раствора диметилаиилина нитритом натри , отличающийс  тем, что реакцию ведут без виешиего охлаждени , примен   Такое разбавление, чтобы образующийс  нитрозопродукт был в растворе. Раство. н-аминоднметиланилина остаПредмет и з о б |) е т о и и  . Способ но;|ученн  нитрозодиметнлmay be large, but must be sifted from dust). When stirring, begin the process; - recover. It should be kept sour reaction all the time, and the parts are given in more hydrochloric acid. By the end of the reduction, the reaction should not be too sour; tone, so as not to form excess amounts of FeCl ;. In total, give: 5i), o-ii acids not more than 38 and with for the whole process of nitrosation and cooling. Tehnor.1tura solution | and by the end of recovery; 1i can reach 30. At the end of Bosstantium, the solution is clear, has a greenish color and gives a weakly lilac color to the Congo, and a light yellow color to the Congo. are worth a day, during which time the game is, 11y1 | The solution of des Sonsetsheino is colorless, which is why it filters it from the cast iron shavings. Pig-iron chips are washed with a small amount of water and this water is poured into the solution of n-aminodimethylaniline. The use of sodium hydroxide with dimethylaylin, a hydrochloric acid solution, is characterized in that the reaction is carried out without supercooling, using such a dilution so that the resulting nitroso product is in solution. Rastvo. n-aminodnmetilanilina ostaPredmet and s about b |) e t about and and. Way but; | scientist nitrosodimetnl

SU29002A 1940-01-13 The method of obtaining nitrosodimethylaniline SU58184A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU29002A SU58184A1 (en) 1940-01-13 The method of obtaining nitrosodimethylaniline

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU29002A SU58184A1 (en) 1940-01-13 The method of obtaining nitrosodimethylaniline

Publications (2)

Publication Number Publication Date
SU19439A1 SU19439A1 (en) 1931-02-28
SU58184A1 true SU58184A1 (en) 1940-10-31

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