RU2010126715A - METHOD FOR PRODUCING 2- AND 4- (1,3,5-DITIAZINAN-5-IL) -PHENOLS - Google Patents

METHOD FOR PRODUCING 2- AND 4- (1,3,5-DITIAZINAN-5-IL) -PHENOLS Download PDF

Info

Publication number
RU2010126715A
RU2010126715A RU2010126715/04A RU2010126715A RU2010126715A RU 2010126715 A RU2010126715 A RU 2010126715A RU 2010126715/04 A RU2010126715/04 A RU 2010126715/04A RU 2010126715 A RU2010126715 A RU 2010126715A RU 2010126715 A RU2010126715 A RU 2010126715A
Authority
RU
Russia
Prior art keywords
dithiazinan
phenols
aminophenol
methyl
ditiazinan
Prior art date
Application number
RU2010126715/04A
Other languages
Russian (ru)
Other versions
RU2443693C1 (en
Inventor
Усеин Меметович Джемилев (RU)
Усеин Меметович Джемилев
Елена Борисовна Рахимова (RU)
Елена Борисовна Рахимова
Инна Владимировна Васильева (RU)
Инна Владимировна Васильева
Внира Рахимовна Ахметова (RU)
Внира Рахимовна Ахметова
Асхат Габдрахманович Ибрагимов (RU)
Асхат Габдрахманович Ибрагимов
Original Assignee
Учреждение Российской академии наук ИНСТИТУТ НЕФТЕХИМИИ И КАТАЛИЗА РАН (RU)
Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран
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 Учреждение Российской академии наук ИНСТИТУТ НЕФТЕХИМИИ И КАТАЛИЗА РАН (RU), Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран filed Critical Учреждение Российской академии наук ИНСТИТУТ НЕФТЕХИМИИ И КАТАЛИЗА РАН (RU)
Priority to RU2010126715/04A priority Critical patent/RU2443693C1/en
Publication of RU2010126715A publication Critical patent/RU2010126715A/en
Application granted granted Critical
Publication of RU2443693C1 publication Critical patent/RU2443693C1/en

Links

Landscapes

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

Abstract

Способ получения 2- и 4-(1,3,5-дитиазинан-5-ил)-фенолов общей формулы (1): ! ! отличающийся тем, что о- или n-аминофенол подвергают взаимодействию с N-метил-1,3,5-дитиазинаном в присутствии катализатора кристаллогидрата нитрата самария [Sm(NO3)2∗6H2O], взятыми в мольном соотношении о-, n-аминофенол:N-метил-1,3,5-дитиазинан:Sm(NO3)2·6H2O=10:(10-12):(0.3-0.7), в атмосфере аргона в среде EtOH-СНСl3 в качестве растворителя при температуре 50-70°С и атмосферном давлении в течение 2.5-3.5 ч. The method of obtaining 2- and 4- (1,3,5-dithiazinan-5-yl) -phenols of the general formula (1):! ! characterized in that o- or n-aminophenol is reacted with N-methyl-1,3,5-dithiazinan in the presence of a samarium nitrate crystalline hydrate catalyst [Sm (NO3) 2 * 6H2O] taken in a molar ratio of o-, n-aminophenol : N-methyl-1,3,5-dithiazinan: Sm (NO3) 2 · 6H2O = 10: (10-12) :( 0.3-0.7), in an argon atmosphere in EtOH-СНСl3 medium as a solvent at a temperature of 50- 70 ° C and atmospheric pressure for 2.5-3.5 hours

Claims (1)

Способ получения 2- и 4-(1,3,5-дитиазинан-5-ил)-фенолов общей формулы (1):The method of obtaining 2- and 4- (1,3,5-dithiazinan-5-yl) -phenols of the general formula (1):
Figure 00000001
Figure 00000001
отличающийся тем, что о- или n-аминофенол подвергают взаимодействию с N-метил-1,3,5-дитиазинаном в присутствии катализатора кристаллогидрата нитрата самария [Sm(NO3)2∗6H2O], взятыми в мольном соотношении о-, n-аминофенол:N-метил-1,3,5-дитиазинан:Sm(NO3)2·6H2O=10:(10-12):(0.3-0.7), в атмосфере аргона в среде EtOH-СНСl3 в качестве растворителя при температуре 50-70°С и атмосферном давлении в течение 2.5-3.5 ч. characterized in that o- or n-aminophenol is reacted with N-methyl-1,3,5-dithiazinan in the presence of a samarium nitrate crystalline hydrate catalyst [Sm (NO 3 ) 2 * 6H 2 O], taken in a molar ratio of o-, n-aminophenol: N-methyl-1,3,5-dithiazinan: Sm (NO 3 ) 2 · 6H 2 O = 10: (10-12) :( 0.3-0.7), in an argon atmosphere in EtOH-CHCl 3 as a solvent at a temperature of 50-70 ° C and atmospheric pressure for 2.5-3.5 hours
RU2010126715/04A 2010-06-29 2010-06-29 Method of producing 2- and 4-(1,3,5-dithiazinan-5-yl)-phenols RU2443693C1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
RU2010126715/04A RU2443693C1 (en) 2010-06-29 2010-06-29 Method of producing 2- and 4-(1,3,5-dithiazinan-5-yl)-phenols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RU2010126715/04A RU2443693C1 (en) 2010-06-29 2010-06-29 Method of producing 2- and 4-(1,3,5-dithiazinan-5-yl)-phenols

Publications (2)

Publication Number Publication Date
RU2010126715A true RU2010126715A (en) 2012-01-10
RU2443693C1 RU2443693C1 (en) 2012-02-27

Family

ID=45783333

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2010126715/04A RU2443693C1 (en) 2010-06-29 2010-06-29 Method of producing 2- and 4-(1,3,5-dithiazinan-5-yl)-phenols

Country Status (1)

Country Link
RU (1) RU2443693C1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2496777C2 (en) * 2012-01-16 2013-10-27 Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран Method for preparing n-(1,5,3-dithiazocynan-3-yl)amides

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE626704A (en) * 1961-12-29
RU2002123631A (en) * 2002-09-04 2004-03-20 ГУ Институт нефтехимии и катализа АН РБ и УНЦ РАН METHOD FOR PRODUCING 5- [ORTO- (META-, PARA-) METHOXYPHENYL] -1,3,5-Dithiazines
RU2291865C1 (en) * 2005-05-13 2007-01-20 Институт нефтехимии и катализа РАН Method for preparing 5-[ortho-(para)-hydroxyphenyl]-1,3,5-dithiazines

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2496777C2 (en) * 2012-01-16 2013-10-27 Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран Method for preparing n-(1,5,3-dithiazocynan-3-yl)amides

Also Published As

Publication number Publication date
RU2443693C1 (en) 2012-02-27

Similar Documents

Publication Publication Date Title
WO2006130280A3 (en) Supports and catalysts comprising rare earth aluminates, and their use in partial oxidation
RU2017117605A (en) METHOD FOR PRODUCING GLYCERINE ACID CARBONATE
MY168414A (en) Catalysts
RU2016133614A (en) METHOD FOR PRODUCING ARILPROPENES
IN2015DN02095A (en)
RU2010126715A (en) METHOD FOR PRODUCING 2- AND 4- (1,3,5-DITIAZINAN-5-IL) -PHENOLS
RU2010122520A (en) METHOD FOR PRODUCING N-Aryl-1,3,5-Dithiazinanes
RU2010108950A (en) METHOD FOR PRODUCING 3,7-DIARIL-1,3,5,7-DITIADIAZAOCTANES
RU2009100738A (en) METHOD FOR PRODUCING 2-PROPYL-3-ETHYLQUINOLINE
RU2012100111A (en) METHOD FOR PRODUCING 2- AND 2,3-SUBSTITUTED QUINOLINS
RU2008152916A (en) METHOD FOR PRODUCING 4- (DIMETHYLAMINO) -2-BUTINYLalkanoates
RU2012101387A (en) METHOD FOR PRODUCING N- (1,5,3-DITIAZOCINAN-3-IL) AMIDES
RU2010132920A (en) METHOD FOR PRODUCING 2-AND 4- (1,3,5-DITIAZINAN-5-IL) -PHENOLS
RU2011121793A (en) METHOD FOR PRODUCING 2- AND 4- (1,5,3-DITIAZOCINAN-3-IL) PHENOLS
RU2008108332A (en) METHOD FOR PRODUCING 2 - [(2-DIMETHYLAMINO) METHYL] PHENOL
RU2008134295A (en) METHOD FOR PRODUCING 1-AMINOMETHYL-ALPHA, OMEGA-ALKADIINS
RU2010137370A (en) METHOD FOR PRODUCING N, N-DIMETHYL-N - [(Alkylsulfanyl) methyl] amines
RU2009103588A (en) METHOD FOR PRODUCING ASYMMETRIC α, ω-DI (AMINOMETHYL) ALKADIINS
RU2008132383A (en) METHOD FOR PRODUCING N1, N1, N4, N4-TETRAMETHYL-2-BUTIN-1,4-DIAMINE
RU2009145363A (en) METHOD FOR PRODUCING TRICYCLIC 2,3,5,6-TETRA-SUBSTITUTED 1,4-Dithiines
RU2012141438A (en) METHOD FOR PRODUCING N- (1,5,3-DITIAZONAN-3-IL) AMIDES
RU2009146601A (en) METHOD FOR PRODUCING N, N-DIMETHYL-5-ALKyl-2-Thiophenamines
RU2007110593A (en) METHOD FOR PRODUCING 1- (DIMETHYLAMINO) -3-ALKyl-2-PROPINOV
RU2010137369A (en) METHOD FOR PRODUCING S, S'-BIS ([N, N-DIMETHYL] METHYL) ALKANDITIOLS
RU2012141437A (en) METHOD FOR SELECTIVE OBTAINING 3,3 '- [METHYLENBIS (1,4-PHENYLENE)] -, 3,3' - [OXYBIS (1,4-PHENYLENE)] - And 3,3 '- (3,3'-DIMETHOXIBIPHENYL- 4,4'-DIIL) -BIS-1,5,3-Dithiazepinanes

Legal Events

Date Code Title Description
MM4A The patent is invalid due to non-payment of fees

Effective date: 20120630