ES2166211T3 - Procedimiento de preparacion de lauril-lactama. - Google Patents
Procedimiento de preparacion de lauril-lactama.Info
- Publication number
- ES2166211T3 ES2166211T3 ES99402108T ES99402108T ES2166211T3 ES 2166211 T3 ES2166211 T3 ES 2166211T3 ES 99402108 T ES99402108 T ES 99402108T ES 99402108 T ES99402108 T ES 99402108T ES 2166211 T3 ES2166211 T3 ES 2166211T3
- Authority
- ES
- Spain
- Prior art keywords
- oxime
- lactama
- lauril
- methanesulfonic acid
- preparation procedure
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D227/00—Heterocyclic compounds containing rings having one nitrogen atom as the only ring hetero atom, according to more than one of groups C07D203/00 - C07D225/00
- C07D227/02—Heterocyclic compounds containing rings having one nitrogen atom as the only ring hetero atom, according to more than one of groups C07D203/00 - C07D225/00 with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
- C07D201/02—Preparation of lactams
- C07D201/04—Preparation of lactams from or via oximes by Beckmann rearrangement
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Cephalosporin Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Abstract
Un procedimiento de preparación de lauril lactama que comprende un proceso en dos etapas de fotonitrosación de ciclododecano y reestructuración de Beckmann de la oxima resultante en presencia de ácido metanosulfónico. La utilización de ácido metanosulfónico como sustituto de ácido sulfúrico en ambas etapas salva los problemas de deposición de oximas y reacciones laterales. La preparación de lauril lactama comprende: (a) Una reacción fotoquímica de ciclododecano, disuelto en un disolvente orgánico, con un agente de nitrosación y cloruro de hidrógeno en presencia de ácido metanosulfónico para formar la oxima de ciclododecanona; y (b) Se somete la oxima a una reestructuración de Beckmann en presencia de ácido metanosulfónico.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9811734A FR2784103B1 (fr) | 1998-09-21 | 1998-09-21 | Procede de preparation de lauryllactame par photonitrosation de cyclododecane et transposition de beckmann en presence d'acide methanesulfonique |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2166211T3 true ES2166211T3 (es) | 2002-04-01 |
Family
ID=9530639
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES99402108T Expired - Lifetime ES2166211T3 (es) | 1998-09-21 | 1999-08-24 | Procedimiento de preparacion de lauril-lactama. |
Country Status (10)
Country | Link |
---|---|
US (1) | US6194570B1 (es) |
EP (1) | EP0989118B1 (es) |
JP (1) | JP3352654B2 (es) |
KR (1) | KR100314982B1 (es) |
CN (1) | CN1191238C (es) |
AT (1) | ATE207464T1 (es) |
CA (1) | CA2282871C (es) |
DE (1) | DE69900383T2 (es) |
ES (1) | ES2166211T3 (es) |
FR (1) | FR2784103B1 (es) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008162935A (ja) * | 2006-12-28 | 2008-07-17 | Daicel Chem Ind Ltd | アミド又はラクタムの製造法 |
FR2931478B1 (fr) * | 2008-05-26 | 2012-08-03 | Arkema France | Prodece de preparation de lactames comprenant une etape de photonitrosation suivie d'une etape de transposition de beckmann |
JP5359063B2 (ja) * | 2008-06-30 | 2013-12-04 | 東レ株式会社 | シクロアルカノンオキシムの製造方法 |
JP5359064B2 (ja) * | 2008-06-30 | 2013-12-04 | 東レ株式会社 | シクロアルカノンオキシムの製造方法および光化学反応装置 |
CN103635457B (zh) | 2012-06-26 | 2015-07-01 | 东丽株式会社 | 环烷酮肟的制造方法 |
EP3498759A1 (de) * | 2017-12-13 | 2019-06-19 | Evonik Degussa GmbH | Verfahren zur herstellung von polymeren aus monomeren umfassend laurinlactam |
EP3498758A1 (de) * | 2017-12-13 | 2019-06-19 | Evonik Degussa GmbH | Verfahren zur herstellung von polymeren aus monomeren umfassend laurinlactam |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2721199A (en) * | 1953-12-15 | 1955-10-18 | Du Pont | Production of amides or lactams from oximes |
FR1335822A (fr) * | 1962-10-09 | 1963-08-23 | Montedison Spa | Procédé de fabrication d'oximes cycloaliphatiques |
FR2417501A1 (fr) * | 1978-02-17 | 1979-09-14 | Ato Chimie | Procede de preparation de lactames par isomerisation d'oximes en milieu sulfurique |
DE3538859A1 (de) * | 1985-11-02 | 1987-05-07 | Huels Chemische Werke Ag | Verfahren zum herstellen von lactamen mit 8 bis 15 kohlenstoffatomen aus den entsprechenden oximen |
FR2746390B1 (fr) * | 1996-03-25 | 1998-04-24 | Atochem Elf Sa | PROCEDE DE PREPARATION DE l'OXIME DE LA CYCLODODECANONE PAR PHOTONITROSATION DE CYCLODODECANE EN PRESENCE DE TRICHLORONITROSOMETHANE |
US6197999B1 (en) * | 1997-07-02 | 2001-03-06 | Atofina | Photonitrosation of cyclododecane in chloroform in quasi-anhydrous medium |
-
1998
- 1998-09-21 FR FR9811734A patent/FR2784103B1/fr not_active Expired - Fee Related
-
1999
- 1999-08-24 ES ES99402108T patent/ES2166211T3/es not_active Expired - Lifetime
- 1999-08-24 EP EP99402108A patent/EP0989118B1/fr not_active Expired - Lifetime
- 1999-08-24 AT AT99402108T patent/ATE207464T1/de not_active IP Right Cessation
- 1999-08-24 DE DE69900383T patent/DE69900383T2/de not_active Expired - Lifetime
- 1999-09-15 KR KR1019990039567A patent/KR100314982B1/ko not_active IP Right Cessation
- 1999-09-20 CA CA002282871A patent/CA2282871C/fr not_active Expired - Fee Related
- 1999-09-21 US US09/400,996 patent/US6194570B1/en not_active Expired - Fee Related
- 1999-09-21 JP JP26701499A patent/JP3352654B2/ja not_active Expired - Fee Related
- 1999-09-21 CN CNB991207106A patent/CN1191238C/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US6194570B1 (en) | 2001-02-27 |
CA2282871C (fr) | 2004-04-13 |
DE69900383T2 (de) | 2002-06-27 |
CA2282871A1 (fr) | 2000-03-21 |
ATE207464T1 (de) | 2001-11-15 |
FR2784103B1 (fr) | 2000-12-08 |
JP2000095756A (ja) | 2000-04-04 |
DE69900383D1 (de) | 2001-11-29 |
CN1191238C (zh) | 2005-03-02 |
KR20000023183A (ko) | 2000-04-25 |
FR2784103A1 (fr) | 2000-04-07 |
KR100314982B1 (ko) | 2001-11-30 |
EP0989118B1 (fr) | 2001-10-24 |
JP3352654B2 (ja) | 2002-12-03 |
EP0989118A1 (fr) | 2000-03-29 |
CN1252404A (zh) | 2000-05-10 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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