AR012004A1 - Procedimento de preparacion de dinitroanilinas 3,4-disustituidas - Google Patents
Procedimento de preparacion de dinitroanilinas 3,4-disustituidasInfo
- Publication number
- AR012004A1 AR012004A1 ARP980101595A ARP980101595A AR012004A1 AR 012004 A1 AR012004 A1 AR 012004A1 AR P980101595 A ARP980101595 A AR P980101595A AR P980101595 A ARP980101595 A AR P980101595A AR 012004 A1 AR012004 A1 AR 012004A1
- Authority
- AR
- Argentina
- Prior art keywords
- disubstituted
- radical
- group
- soluble salts
- carried out
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- -1 3,4-disubstituted dinitroanilines Chemical class 0.000 abstract 6
- 150000003839 salts Chemical class 0.000 abstract 2
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical compound F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 abstract 1
- 238000010934 O-alkylation reaction Methods 0.000 abstract 1
- XIPUIGPNIDKXJU-UHFFFAOYSA-N [CH]1CC1 Chemical compound [CH]1CC1 XIPUIGPNIDKXJU-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229940100198 alkylating agent Drugs 0.000 abstract 1
- 239000002168 alkylating agent Substances 0.000 abstract 1
- 238000005576 amination reaction Methods 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 150000002500 ions Chemical class 0.000 abstract 1
- 230000000802 nitrating effect Effects 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 239000012429 reaction media Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 229910052723 transition metal Inorganic materials 0.000 abstract 1
- 150000003624 transition metals Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/14—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups
- C07C209/18—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups with formation of amino groups bound to carbon atoms of six-membered aromatic rings or from amines having nitrogen atoms bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Procedimiento de propagacion de dinitroanilinas 3,4-disustituidas de formula 1 en la cual R1 y R2 que son idénticos o diferentes el uno del otro,representan un átomo de hidrogeno, un radical alquilo rectilíneo o ramificado saturado con C, aC6, un radical alquileno lineal o ramificado con C2 a C6, unradical ciclopropilo o un radical cloroetilo. R3 y R4 que pueden ser idénticos o diferentes el uno del otro, se eligen en el grupo que comprende el átomo decloro, el grupo amino, losradica les alquilo inferiores con C1 a C3y el radical trifluorometilo, que comprende sucesivamente una etapa de dnitracion de unfenol; 3,4-disustituido, una etapa de aminacion del 2,6-dinitro-alcoxibenceno 3,4-disustituido así obtenido ycaracterizado por que: La etapa de dinitraciondel fenol 3,4-disustituido correspondiente a la dinitroanilina 3,4-disustituida buscada, se efectua en el seno de un medio de reaccion que comprende un pequenoexceso de apente nitrante, una cantidadsuficiente de protones y un catalizador elegido en el grupo que comprende las sales solubles de los metales detransicion de las columnas IV a XII de la clasificacion periodica, preferentemente las sales solubles de los iones Fe+++,Fe++, Zn++, Cn++ yporque una etapa de O-alquilacio del fenol 3,4 disustituido dinitrado obtenido en la etapa anterior, se efectua con la ayuda de un agente alquilante.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9704235A FR2761684B1 (fr) | 1997-04-07 | 1997-04-07 | Procede de preparation des dinitroanilines 3,4-disubstituees |
| FR9708359A FR2765575B1 (fr) | 1997-07-02 | 1997-07-02 | Procede de preparation des dinitroanilines 3,4-disubstituees |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR012004A1 true AR012004A1 (es) | 2000-09-13 |
Family
ID=26233452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP980101595A AR012004A1 (es) | 1997-04-07 | 1998-04-07 | Procedimento de preparacion de dinitroanilinas 3,4-disustituidas |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6028226A (es) |
| EP (1) | EP0870756B1 (es) |
| CN (1) | CN1197058A (es) |
| AR (1) | AR012004A1 (es) |
| AT (1) | ATE208368T1 (es) |
| AU (1) | AU6067098A (es) |
| BR (1) | BR9801379A (es) |
| DE (1) | DE69802329D1 (es) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20160035081A (ko) | 2013-08-07 | 2016-03-30 | 애로우헤드 리서치 코오포레이션 | 생체 내에서 RNAi 유발제를 종양 세포로 전달하기 위한 폴리콘주게이트 |
| CN104592043A (zh) * | 2014-12-29 | 2015-05-06 | 浙江龙盛集团股份有限公司 | 一种连续化合成2,6-二氯对硝基苯胺的清洁工艺 |
| CN104592042A (zh) * | 2014-12-29 | 2015-05-06 | 浙江龙盛集团股份有限公司 | 一种连续化合成2,4-二硝基-6-氯苯胺的清洁工艺 |
| CN114409576A (zh) * | 2021-12-22 | 2022-04-29 | 中国石油天然气集团有限公司 | 一种芳基磺酸盐表面活性剂及其制备方法 |
| CN117049967B (zh) * | 2023-07-10 | 2025-12-19 | 西华大学 | 2,6-二硝基-3,4-二甲基苯酚衍生物的制备方法及活性应用 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL106118A (en) * | 1993-06-24 | 1997-08-14 | Agan Chemical Manufacturers | Process for preparing n-alkyl-3,4-dialkyl- 2,6-dinitro- anilines and intermediates thereof |
| US5689006A (en) * | 1995-06-29 | 1997-11-18 | Srm Chemical, Ltd. Co. | Process for producing n-alkyl-dinitroalkylanilines |
-
1998
- 1998-04-06 EP EP98400820A patent/EP0870756B1/fr not_active Expired - Lifetime
- 1998-04-06 DE DE69802329T patent/DE69802329D1/de not_active Expired - Lifetime
- 1998-04-06 AT AT98400820T patent/ATE208368T1/de not_active IP Right Cessation
- 1998-04-06 AU AU60670/98A patent/AU6067098A/en not_active Abandoned
- 1998-04-07 CN CN98108049A patent/CN1197058A/zh active Pending
- 1998-04-07 BR BR9801379A patent/BR9801379A/pt not_active IP Right Cessation
- 1998-04-07 AR ARP980101595A patent/AR012004A1/es active IP Right Grant
- 1998-04-07 US US09/056,415 patent/US6028226A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US6028226A (en) | 2000-02-22 |
| EP0870756B1 (fr) | 2001-11-07 |
| BR9801379A (pt) | 1999-05-18 |
| ATE208368T1 (de) | 2001-11-15 |
| EP0870756A1 (fr) | 1998-10-14 |
| CN1197058A (zh) | 1998-10-28 |
| DE69802329D1 (de) | 2001-12-13 |
| AU6067098A (en) | 1998-10-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration |