RU2003126271A - METHOD FOR PRODUCING N-SUBSTITUTED LACTAMS - Google Patents

METHOD FOR PRODUCING N-SUBSTITUTED LACTAMS Download PDF

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Publication number
RU2003126271A
RU2003126271A RU2003126271/04A RU2003126271A RU2003126271A RU 2003126271 A RU2003126271 A RU 2003126271A RU 2003126271/04 A RU2003126271/04 A RU 2003126271/04A RU 2003126271 A RU2003126271 A RU 2003126271A RU 2003126271 A RU2003126271 A RU 2003126271A
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RU
Russia
Prior art keywords
chloro
lactams
producing
substituted lactams
substituted
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RU2003126271/04A
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Russian (ru)
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RU2246487C9 (en
RU2246487C1 (en
Inventor
Ирина Александровна Хардина (RU)
Ирина Александровна Хардина
Тамара Петровна Алейникова (RU)
Тамара Петровна Алейникова
Олег Иванович Тужиков (RU)
Олег Иванович Тужиков
Инга Юрьевна Ковалец (RU)
Инга Юрьевна Ковалец
В чеслав Евгеньевич Дербишер (RU)
Вячеслав Евгеньевич Дербишер
Анатолий Николаевич Попов (RU)
Анатолий Николаевич Попов
Original Assignee
Волгоградский государственный технический университет (ВолгГТУ) (RU)
Волгоградский государственный технический университет (ВолгГТУ)
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Priority to RU2003126271/04A priority Critical patent/RU2246487C9/en
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Publication of RU2246487C1 publication Critical patent/RU2246487C1/en
Publication of RU2003126271A publication Critical patent/RU2003126271A/en
Publication of RU2246487C9 publication Critical patent/RU2246487C9/en

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  • Hydrogenated Pyridines (AREA)
  • Pyrrole Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Claims (1)

Способ получения N-замещенных лактамов общей формулы:The method of obtaining N-substituted lactams of the General formula:
Figure 00000001
Figure 00000001
где R=Н, Cl,where R = H, Cl, R’=(СН2)3, (СН2)5,R '= (CH 2 ) 3 , (CH 2 ) 5 , заключающийся в присоединении N-хлорлактамов к аллилбензолу, причем в качестве N-хлорлактамов используют N-хлорбутиролактам или N-хлоркапролактам, процесс проводят при мольном соотношении N-хлорлактама и аллилбензола, равном 1-1,15:1, в присутствии катализатора моно-трет-бутилперокси-α-метилметоксиэтоксиэтилового эфира этиленгликоля, взятого в количестве 0,4-4,0% масс., в среде инертного растворителя, например, хлорбензола при температуре 100-125°С в течение 15-20 минут.consisting in the addition of N-chloro-lactams to allylbenzene, with N-chloro-butyrolactam or N-chloro-caprolactam being used as N-chloro-lactams, the process is carried out at a molar ratio of N-chloro-lactam and allyl-benzene equal to 1-1.15: 1 in the presence of a mono-tert catalyst -butylperoxy-α-methylmethoxyethoxyethyl ether of ethylene glycol, taken in an amount of 0.4-4.0 wt.%, in an inert solvent, for example, chlorobenzene at a temperature of 100-125 ° C for 15-20 minutes.
RU2003126271/04A 2003-08-27 2003-08-27 Method for preparing n-substituted lactams RU2246487C9 (en)

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RU2003126271/04A RU2246487C9 (en) 2003-08-27 2003-08-27 Method for preparing n-substituted lactams

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RU2003126271/04A RU2246487C9 (en) 2003-08-27 2003-08-27 Method for preparing n-substituted lactams

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RU2246487C1 RU2246487C1 (en) 2005-02-20
RU2003126271A true RU2003126271A (en) 2005-02-27
RU2246487C9 RU2246487C9 (en) 2006-02-20

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RU2246487C9 (en) 2006-02-20
RU2246487C1 (en) 2005-02-20

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