SU259848A1 - Method of preparing borazole - Google Patents

Method of preparing borazole Download PDF

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Publication number
SU259848A1
SU259848A1 SU681262721A SU1262721A SU259848A1 SU 259848 A1 SU259848 A1 SU 259848A1 SU 681262721 A SU681262721 A SU 681262721A SU 1262721 A SU1262721 A SU 1262721A SU 259848 A1 SU259848 A1 SU 259848A1
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SU
USSR - Soviet Union
Prior art keywords
borazole
borohydride
preparing
ammonium chloride
heated
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Application number
SU681262721A
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Russian (ru)
Inventor
В.В. Волков
Г.И. Багрянцев
Л.Н. Рагозин
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Институт Неорганической Химии Со Ан Ссср
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Priority to SU681262721A priority Critical patent/SU259848A1/en
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Publication of SU259848A1 publication Critical patent/SU259848A1/en

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Description

Изобретение относитс  к способу получени  боразола, который может быть использован в качестве исходного продукта при синтезе борорганических соединений в препаративной. химии и в радиометрических приборах, как индикаторный газ дл  нейтронов.The invention relates to a process for the preparation of borazole, which can be used as a starting material in the synthesis of organoboron compounds in preparative. chemistry and radiometric devices, as an indicator gas for neutrons.

Известен способ получени  боразола путем нагревани  смеси боргидрида лити  с хлористым аммонием в присутствии измельченного стекла перикс при температуре 220-300СA method of producing borazol is known by heating a mixture of lithium borohydride and ammonium chloride in the presence of crushed perix glass at a temperature of 220-300 ° C.

Дл  упрощени  способа предлагаетс  в качестве боргидрида щелочного металла использовать боргидрид натри и процесс нагревани  проводить при интенсивном истирании реагентов.To simplify the process, it is proposed to use sodium borohydride as the alkali metal borohydride and to carry out the heating process with intensive abrasion of the reactants.

При осуществлении этого способа температура процесса понижаетс  до 150-230°С. Дл  процесса используют менее дефицитный реагент.When implementing this method, the process temperature is reduced to 150-230 ° C. A less deficient reagent is used for the process.

. П Р и м е р. Во вращающийс  стальной реактор объемом 0,7 л, заполненный на 50% истирающей насадкой. PRIMER. A 0.7 l rotating steel reactor filled to 50% with an abrasive nozzle

в виде металлических пиров, загружают 12 г боргидрида натри  и 18 г сухого хлористого аммони .in the form of metal peers, 12 g of sodium borohydride and 18 g of dry ammonium chloride are loaded.

Реактор герметизируют, откачивают атмосферный воздух до остаточного давлени  0,1 мм рт.ст. и нагревают сначала до температуры 150 С, а затем через 0,5-1 ч до 200-230 С. Образующиес  газообразные продукты реакции нагревают в охлаждаемле жидким азотом ловушки-конденсаторы, в которлх отдел ют боразол от водорода . Выход боразола 23%.The reactor is sealed, atmospheric air is evacuated to a residual pressure of 0.1 mm Hg. and firstly heated to a temperature of 150 ° C, and then in 0.5-1 hours to 200-230 ° C. The resulting gaseous reaction products are heated in cooled with liquid nitrogen, traps-condensers, in which borazole is separated from hydrogen. The output of borazole 23%.

Claims (1)

Формула изобретени Invention Formula Способ получени  боразола путем обработки боргидрида щелочного мета.гта хлористым аммонием при нагревании , отлич ающийс  тем, что, с целью упрощени  способа в качестве боргидрида щелочного металла берут боргидрид натри  и процесс нагревани  провод т при интсивном истирании реагентов.The method of producing borazole by treating an alkali metagt borohydride with ammonium chloride when heated, is characterized in that, in order to simplify the process, sodium borohydride is taken as the alkali metal borohydride and the heating process is carried out with intensive abrasion of the reagents.
SU681262721A 1968-08-03 1968-08-03 Method of preparing borazole SU259848A1 (en)

Priority Applications (1)

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SU681262721A SU259848A1 (en) 1968-08-03 1968-08-03 Method of preparing borazole

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SU681262721A SU259848A1 (en) 1968-08-03 1968-08-03 Method of preparing borazole

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5612013A (en) * 1995-02-10 1997-03-18 Trustees Of The University Of Pennsylvania Method for synthesis of borazine

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5612013A (en) * 1995-02-10 1997-03-18 Trustees Of The University Of Pennsylvania Method for synthesis of borazine

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