RU2011121793A - METHOD FOR PRODUCING 2- AND 4- (1,5,3-DITIAZOCINAN-3-IL) PHENOLS - Google Patents

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

Info

Publication number
RU2011121793A
RU2011121793A RU2011121793/04A RU2011121793A RU2011121793A RU 2011121793 A RU2011121793 A RU 2011121793A RU 2011121793/04 A RU2011121793/04 A RU 2011121793/04A RU 2011121793 A RU2011121793 A RU 2011121793A RU 2011121793 A RU2011121793 A RU 2011121793A
Authority
RU
Russia
Prior art keywords
propanedithiol
aminophenol
formaldehyde
phenols
room temperature
Prior art date
Application number
RU2011121793/04A
Other languages
Russian (ru)
Other versions
RU2478627C2 (en
Inventor
Усеин Меметович Джемилев
Елена Борисовна Рахимова
Инна Владимировна Васильева
Василий Михайлович Яныбин
Асхат Габдрахманович Ибрагимов
Original Assignee
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 filed Critical Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран
Priority to RU2011121793/04A priority Critical patent/RU2478627C2/en
Publication of RU2011121793A publication Critical patent/RU2011121793A/en
Application granted granted Critical
Publication of RU2478627C2 publication Critical patent/RU2478627C2/en

Links

Landscapes

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

Abstract

Способ получения 2- и 4-(1,5,3-дитиазоцинан-3-ил)фенолов общей формулы (1):отличающийся тем, что формальдегид предварительно перемешивают с 1,3-пропандитиолом при комнатной (~20°C) температуре в течение 30 мин с последующим добавлением о-, n-аминофенола в EtOH в качестве растворителя в присутствии катализатора кристаллогидрата нитрата самария Sm(NO)·6HO при мольном соотношении формальдегид: 1,3-пропандитиол: о-, n-аминофенол: Sm(NO)·6HO=20:10:10:(0.3-0.7) в атмосфере аргона при комнатной (~20°C) температуре и атмосферном давлении в течение 2.5-3.5 ч. The method of obtaining 2- and 4- (1,5,3-dithiazocinan-3-yl) phenols of the general formula (1): characterized in that formaldehyde is pre-mixed with 1,3-propanedithiol at room temperature (~ 20 ° C) at for 30 min followed by the addition of o-, n-aminophenol in EtOH as a solvent in the presence of a samarium nitrate crystalline hydrate catalyst Sm (NO) · 6HO with a molar ratio of formaldehyde: 1,3-propanedithiol: o-, n-aminophenol: Sm (NO ) · 6HO = 20: 10: 10: (0.3-0.7) in an argon atmosphere at room temperature (~ 20 ° C) and atmospheric pressure for 2.5-3.5 hours.

Claims (1)

Способ получения 2- и 4-(1,5,3-дитиазоцинан-3-ил)фенолов общей формулы (1):The method of obtaining 2- and 4- (1,5,3-dithiazocinan-3-yl) phenols of the general formula (1):
Figure 00000001
Figure 00000001
отличающийся тем, что формальдегид предварительно перемешивают с 1,3-пропандитиолом при комнатной (~20°C) температуре в течение 30 мин с последующим добавлением о-, n-аминофенола в EtOH в качестве растворителя в присутствии катализатора кристаллогидрата нитрата самария Sm(NO3)3·6H2O при мольном соотношении формальдегид: 1,3-пропандитиол: о-, n-аминофенол: Sm(NO3)3·6H2O=20:10:10:(0.3-0.7) в атмосфере аргона при комнатной (~20°C) температуре и атмосферном давлении в течение 2.5-3.5 ч. characterized in that formaldehyde is pre-mixed with 1,3-propanedithiol at room temperature (~ 20 ° C) for 30 minutes, followed by the addition of o-, n-aminophenol in EtOH as a solvent in the presence of a samarium nitrate crystalline hydrate catalyst Sm (NO 3 ) 3 · 6H 2 O with a molar ratio of formaldehyde: 1,3-propanedithiol: o-, n-aminophenol: Sm (NO 3 ) 3 · 6H 2 O = 20: 10: 10: (0.3-0.7) in argon atmosphere at room (~ 20 ° C) temperature and atmospheric pressure for 2.5-3.5 hours
RU2011121793/04A 2011-05-30 2011-05-30 Method for preparing 2- and 4-(1,5,3-dithiazocynan-3-yl)phenols RU2478627C2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
RU2011121793/04A RU2478627C2 (en) 2011-05-30 2011-05-30 Method for preparing 2- and 4-(1,5,3-dithiazocynan-3-yl)phenols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RU2011121793/04A RU2478627C2 (en) 2011-05-30 2011-05-30 Method for preparing 2- and 4-(1,5,3-dithiazocynan-3-yl)phenols

Publications (2)

Publication Number Publication Date
RU2011121793A true RU2011121793A (en) 2012-12-10
RU2478627C2 RU2478627C2 (en) 2013-04-10

Family

ID=49152468

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2011121793/04A RU2478627C2 (en) 2011-05-30 2011-05-30 Method for preparing 2- and 4-(1,5,3-dithiazocynan-3-yl)phenols

Country Status (1)

Country Link
RU (1) RU2478627C2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2559361C1 (en) * 2014-04-04 2015-08-10 Федеральное государственное бюджетное учреждение науки Институт нефтехимии и катализа Российской академии наук Method of producing n-aryl-1,5,3-dithiazonanes

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2291865C1 (en) * 2005-05-13 2007-01-20 Институт нефтехимии и катализа РАН Method for preparing 5-[ortho-(para)-hydroxyphenyl]-1,3,5-dithiazines

Also Published As

Publication number Publication date
RU2478627C2 (en) 2013-04-10

Similar Documents

Publication Publication Date Title
MX2022007264A (en) Enhancing autophagy or increasing longevity by administration of urolithins or precursors thereof.
RU2011121793A (en) METHOD FOR PRODUCING 2- AND 4- (1,5,3-DITIAZOCINAN-3-IL) PHENOLS
PH12017500382A1 (en) Method for purifying plant-derived carbon percursor
RU2012100111A (en) METHOD FOR PRODUCING 2- AND 2,3-SUBSTITUTED QUINOLINS
RU2010122520A (en) METHOD FOR PRODUCING N-Aryl-1,3,5-Dithiazinanes
RU2011123582A (en) METHOD FOR PRODUCING 3- (o-, m-, p-METHOXYPHENYL) -TETRAHYDRO-2H-1, 5, 3-DIOXAZEPINES
RU2012145705A (en) METHOD FOR PRODUCING 3-Pyridinyl-1,5,3-Dithiazepinanes
RU2012145638A (en) METHOD FOR PRODUCING 3-Pyridinyl-1,5,3-Dithiazocinanes
RU2010122542A (en) METHOD FOR PRODUCING MONO- (DI-, TETRA-) METHYL-1,2-BIS- (1,3,5-DITIAZINAN-5-IL) ETHANES
RU2010126715A (en) METHOD FOR PRODUCING 2- AND 4- (1,3,5-DITIAZINAN-5-IL) -PHENOLS
RU2012147376A (en) METHOD FOR PRODUCING 3,3-DI (METHOXICARBONIL) -1,5-DITIACYCLOalkanes
RU2011124568A (en) METHOD FOR PRODUCING α, ω-BIS- (1,5,3-DITIAZEPINAN-3-IL) ALKANOV
RU2012144046A (en) METHOD FOR PRODUCING α, ω- {BIS [(PENTAN-2,4-DION-3-IL) METHYL SULFANIL]} - ALKANOV
RU2012141442A (en) METHOD FOR PRODUCING 3, 3 '- [OXA (TIA) ALKAN-α, ω-DIIL] -BIS-1,5,3-Dithiazepinanes
RU2013152020A (en) METHOD FOR PRODUCING (1,5,3-DITIAZEPAN-3-IL) -ALKANDIOLS
RU2012144636A (en) METHOD FOR PRODUCING 4- (1,5,3-Dithiazepinan-3-yl) -benzoic and 5- (1,5,3-dithiazepinan-3-yl) -2-hydroxybenzoic acid
RU2011121794A (en) METHOD FOR PRODUCING (1,5,3-DITIAZEPINAN-3-IL) (THIO) PHENOLS
RU2011127306A (en) METHOD FOR PRODUCING 3- (m-, p-METHYLPHENYL) -1,5,3-Dithiazepanes
IN2012DN00346A (en)
RU2011130061A (en) METHOD FOR PRODUCING ALKYL ETHERS OF BENZOIC ACID
RU2010104333A (en) METHOD FOR PRODUCING DIOCTIL ETHER
RU2014113764A (en) METHOD FOR PRODUCING N-Aryl-1,5,3-Dithiazekanes
RU2014114559A (en) METHOD FOR PRODUCING N-Aryl-1,5,3-Dithiazacacycloundecanes
RU2013122018A (en) METHOD FOR PRODUCING 1-AZIDO-2-ETHYL-1,2-DIHYDROS (С60-Ih) [5,6] FULLERENA
RU2013146152A (en) METHOD FOR PRODUCING DISULFANILETETRACYCLOalkenes

Legal Events

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

Effective date: 20130531