SU108135A1 - The method of obtaining organic compounds containing sulfur and nitrogen - Google Patents

The method of obtaining organic compounds containing sulfur and nitrogen

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Publication number
SU108135A1
SU108135A1 SU551266A SU551266A SU108135A1 SU 108135 A1 SU108135 A1 SU 108135A1 SU 551266 A SU551266 A SU 551266A SU 551266 A SU551266 A SU 551266A SU 108135 A1 SU108135 A1 SU 108135A1
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SU
USSR - Soviet Union
Prior art keywords
nitrogen
organic compounds
compounds containing
containing sulfur
obtaining organic
Prior art date
Application number
SU551266A
Other languages
Russian (ru)
Inventor
Кальтвассер Ганс
Реклинг Гергард
Тиль Макс
Азингер Фридрих
Original Assignee
Кальтвассер Ганс
Реклинг Гергард
Тиль Макс
Азингер Фридрих
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
Application filed by Кальтвассер Ганс, Реклинг Гергард, Тиль Макс, Азингер Фридрих filed Critical Кальтвассер Ганс
Priority to SU551266A priority Critical patent/SU108135A1/en
Application granted granted Critical
Publication of SU108135A1 publication Critical patent/SU108135A1/en

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Description

Предла1-аетс  способ получении органических соединений, содерл ащих азот и серу, сущност которого состоит в том, что соединени5т, содержагиие кето-группу, ввод т во взаимодействие с серой или иолисульфидом при одновременном воздействии аммиака. По.лученные соединени  представл ют собой ценные промежуточные или готовые продукты дл  фармацевтичееко иромьпп.пенности. Кроме того, эти продукты могут найти применение в качестве средств дл  борьбы с з|)едител ми, дл  уничтожени  еорных трав, дл  запшты против ржавчины и старени .A method is proposed for the preparation of organic compounds containing nitrogen and sulfur, the essence of which is that the compound containing a keto group is brought into contact with sulfur or iolysulfide with simultaneous exposure to ammonia. The resulting compounds are valuable intermediates or finished products for the pharmaceutical industry. In addition, these products can be used as a means for combating s | | with agents, for the destruction of eorian herbs, for rust and aging.

Описываемы.й способ ио.тучени  названных соединений осуществл етс  следующим образом.The described procedure for the etching process of the named compounds is carried out as follows.

Во взвесь из 1 мол  серы и 2 молей кето-соедипени  ввод т при комнатной температуре аммиачный газ. Способ может быть осуществ .leH также и в присутствии растворителей , например спирта, бензола, различных эфиров и друтих соединений . Вместо ееры может быть применен полисульфид, например,A suspension of ammonium gas from 1 mol of sulfur and 2 moles of keto-compound is introduced at room temperature. The method can also be carried out. LeH in the presence of solvents, for example alcohol, benzene, various esters and other compounds. Polysulfide can be used instead of eera, for example,

г.ммонии, натри , а также и органические полисульфиды, например, .теновьп полисульфид.ammonium, sodium, as well as organic polysulfides, for example, .two polysulfide.

Б качестве кего-соеди} ени 1 могут использованы все кетоны, в.хо;|ЯП1ИС в форму., , --- СМ - СО -- СМ2--Rs, где RI Ra ; Rs могут водородом.All ketones, w.cho; | ЯП1ИС in the form.,, --- СМ - СО - СМ2 - Rs, where RI Ra; Rs can be hydrogen.

пример 1. С меипшают 144 г люти.-эгплкетома с 32 г серы (серного цвета м.ти по|.1он1ка черенково се;;ы).. В чту взвесь ввод т амглиачны: газ до тех нор, пока сера не перейдет в раетпор; при этом А оже1 нроизводитье  подогрев до 80°. К темно-коричневой реакционной смеси прибавл ют эфир и щелочной раствор г ромьшают водой. Пр1-5 дистил .1 н,ии освобожденпо от фира части получепно1о продукта выдел ют 135 г соединени  состава ( с темпсрату;)ой кипени  70°. Выход составл ет 85% от теоретического .Example 1. With 144 g of lute.-egplequtome with 32 g of sulfur (sulfur-gray, m. ti | .111ka cherenkovo se ;; s). raetpor; at the same time, the Auger1 produces heating up to 80 °. Ether is added to the dark brown reaction mixture and the alkaline solution is rinsed with water. Ex. 1–5 distillate .1 n, o and freed from the portion of the receptacle product, 135 g of the compound of the composition (with temperature; boiling point 70 °) were isolated. The yield is 85% of theoretical.

Пример 2. Ввод т 196 г циклогексаиона в водный раствор полису Пзфида натри . Эта смесь при тщательном размешивании обрабаТглваетс  в течение 2 часов приExample 2. 196 g of cyclohexaion are added to an aqueous solution of Pzfida sodium. This mixture, while thoroughly stirring, is processed for 2 hours at

SU551266A 1956-05-04 1956-05-04 The method of obtaining organic compounds containing sulfur and nitrogen SU108135A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU551266A SU108135A1 (en) 1956-05-04 1956-05-04 The method of obtaining organic compounds containing sulfur and nitrogen

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU551266A SU108135A1 (en) 1956-05-04 1956-05-04 The method of obtaining organic compounds containing sulfur and nitrogen

Publications (1)

Publication Number Publication Date
SU108135A1 true SU108135A1 (en) 1956-11-30

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Country Status (1)

Country Link
SU (1) SU108135A1 (en)

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