RU2010133701A - METHOD FOR PRODUCING 1,3,5-THIADIAZINAN-4- (TI) ON - Google Patents

METHOD FOR PRODUCING 1,3,5-THIADIAZINAN-4- (TI) ON Download PDF

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RU2010133701A
RU2010133701A RU2010133701/04A RU2010133701A RU2010133701A RU 2010133701 A RU2010133701 A RU 2010133701A RU 2010133701/04 A RU2010133701/04 A RU 2010133701/04A RU 2010133701 A RU2010133701 A RU 2010133701A RU 2010133701 A RU2010133701 A RU 2010133701A
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Russia
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buona
carbamide
thio
thiadiazinan
butanol
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RU2010133701/04A
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Russian (ru)
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RU2447067C1 (en
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Усеин Меметович Джемилев (RU)
Усеин Меметович Джемилев
Внира Рахимовна Ахметова (RU)
Внира Рахимовна Ахметова
Регина Радиевна Хайруллина (RU)
Регина Радиевна Хайруллина
Асхат Габдрахманович Ибрагимов (RU)
Асхат Габдрахманович Ибрагимов
Райхана Валиулловна Кунакова (RU)
Райхана Валиулловна Кунакова
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Учреждение Российской академии наук ИНСТИТУТ НЕФТЕХИМИИ И КАТАЛИЗА РАН (RU)
Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран
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  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Способ получения 1,3,5-тиадиазинан-4-(ти)онов общей формулы (1): ! ! отличающийся тем, что насыщенный сероводородом водный 37%-ный раствор формальдегида подвергают взаимодействию со свежеприготовленной смесью (тио)карбамид - н-BuONa (в бутаноле) при мольном соотношении исходных реагентов (тио)карбамид:CH2O:H2S:н-BuONa, равном 10:20:20:40 при температуре 70-90°C и атмосферном давлении в течение 5-7 ч. The method of obtaining 1,3,5-thiadiazinan-4- (ty) ones of the general formula (1):! ! characterized in that the aqueous 37% solution of formaldehyde saturated with hydrogen sulfide is reacted with a freshly prepared mixture of (thio) carbamide - n-BuONa (in butanol) at a molar ratio of the starting reagents (thio) carbamide: CH2O: H2S: n-BuONa equal to 10 : 20: 20: 40 at a temperature of 70-90 ° C and atmospheric pressure for 5-7 hours

Claims (1)

Способ получения 1,3,5-тиадиазинан-4-(ти)онов общей формулы (1):The method of obtaining 1,3,5-thiadiazinan-4- (ty) ones of the general formula (1):
Figure 00000001
Figure 00000001
отличающийся тем, что насыщенный сероводородом водный 37%-ный раствор формальдегида подвергают взаимодействию со свежеприготовленной смесью (тио)карбамид - н-BuONa (в бутаноле) при мольном соотношении исходных реагентов (тио)карбамид:CH2O:H2S:н-BuONa, равном 10:20:20:40 при температуре 70-90°C и атмосферном давлении в течение 5-7 ч. characterized in that the aqueous 37% solution of formaldehyde saturated with hydrogen sulfide is reacted with a freshly prepared mixture of (thio) carbamide - n-BuONa (in butanol) at a molar ratio of the starting reagents (thio) carbamide: CH 2 O: H 2 S: n- BuONa, equal to 10: 20: 20: 40 at a temperature of 70-90 ° C and atmospheric pressure for 5-7 hours.
RU2010133701/04A 2010-08-11 2010-08-11 Method of producing 1,3,5-thiadiazinan-4-(thi)ones RU2447067C1 (en)

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Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL104081A (en) * 1991-12-21 1996-05-14 Basf Ag Preparation of substantially dust-free tetrahydro-3, 5-dimethyl-1, 3, 5-thiadiazine-2-thione granules
KR100329700B1 (en) * 1994-12-30 2002-10-25 주식회사 엘지씨아이 Process for preparing tetrahydro-1,3,5-thiadiazin-4-one

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