GB902570A - Preparation of c-alkylated piperazines - Google Patents
Preparation of c-alkylated piperazinesInfo
- Publication number
- GB902570A GB902570A GB3194158A GB3194158A GB902570A GB 902570 A GB902570 A GB 902570A GB 3194158 A GB3194158 A GB 3194158A GB 3194158 A GB3194158 A GB 3194158A GB 902570 A GB902570 A GB 902570A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxide
- preparation
- atmospheres
- alkyl radical
- catalyst
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/023—Preparation; Separation; Stabilisation; Use of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
In a process for preparing C-alkylated piperazines, a dialkanolamine of the formula: Z.CHOH.CHR1.NH.CRR11.CHR111.OH, in which Z is C1-10 alkyl radical and R, R1, R11 and R111 are each a hydrogen atom or a C1-3 alkyl radical, is reacted at an elevated temperature and under a pressure within a range of 30 to 400 atmospheres with ammonia in the presence of hydrogen having a partial pressure of 10 to 200 atmospheres and a hydrogenation catalyst which comprises at least one metal or oxide of nickel, copper or cobalt. The catalyst may optionally contain a minor amount of a promoter which is chromium oxide, molybdenum oxide, manganese oxide or thorium oxide or a mixture thereof. Tetramethyl pyrazine is also formed as a byproduct in the preparation of 2,3,5,6-tetramethylpiperazine. 1-(2-Hydroxyethylamino)-2-dodecanol is prepared from dodecene oxide and monoethanolamine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US69019957A | 1957-10-15 | 1957-10-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB902570A true GB902570A (en) | 1962-08-01 |
Family
ID=24771517
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3194158A Expired GB902570A (en) | 1957-10-15 | 1958-10-07 | Preparation of c-alkylated piperazines |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1140939B (en) |
FR (1) | FR1206423A (en) |
GB (1) | GB902570A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0235651A1 (en) * | 1986-02-18 | 1987-09-09 | BASF Aktiengesellschaft | Process for the preparation of N-methylpiperazine |
EP0446783A2 (en) * | 1990-03-15 | 1991-09-18 | BASF Aktiengesellschaft | Procedure for the preparation of N-aryl substituted 2-aminoalkyl-2-hydroxyalkylamines and N-aryl substituted piperazines |
EP1031568A1 (en) * | 1999-02-24 | 2000-08-30 | Bayer Aktiengesellschaft | Process for the preparation of cis-Dimethylpiperazine |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2525223A (en) * | 1948-05-25 | 1950-10-10 | American Cyanamid Co | Preparation of n-substituted piperazines |
-
1958
- 1958-10-07 GB GB3194158A patent/GB902570A/en not_active Expired
- 1958-10-11 DE DE1958I0015507 patent/DE1140939B/en active Pending
- 1958-10-14 FR FR1206423D patent/FR1206423A/en not_active Expired
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0235651A1 (en) * | 1986-02-18 | 1987-09-09 | BASF Aktiengesellschaft | Process for the preparation of N-methylpiperazine |
US4845218A (en) * | 1986-02-18 | 1989-07-04 | Basf Aktiengesellschaft | Preparation of n-methylpiperazine |
EP0446783A2 (en) * | 1990-03-15 | 1991-09-18 | BASF Aktiengesellschaft | Procedure for the preparation of N-aryl substituted 2-aminoalkyl-2-hydroxyalkylamines and N-aryl substituted piperazines |
EP0446783A3 (en) * | 1990-03-15 | 1991-11-27 | Basf Aktiengesellschaft | Procedure for the preparation of n-aryl substituted 2-aminoalkyl-2-hydroxyalkylamines and n-aryl substituted piperazines |
US5110928A (en) * | 1990-03-15 | 1992-05-05 | Basf Aktiengesellschaft | Preparation of n-aryl-substituted 2-aminoalkyl-2-hydroxyalkylamines and n-aryl-substituted piperazines |
EP1031568A1 (en) * | 1999-02-24 | 2000-08-30 | Bayer Aktiengesellschaft | Process for the preparation of cis-Dimethylpiperazine |
DE19907829A1 (en) * | 1999-02-24 | 2000-08-31 | Bayer Ag | Process for the preparation of cis-2,6-dimethylpiperazine |
DE19907829C2 (en) * | 1999-02-24 | 2001-05-10 | Bayer Ag | Process for the preparation of cis-2,6-dimethylpiperazine |
US6316622B1 (en) | 1999-02-24 | 2001-11-13 | Bayer Aktiengesellschaft | Process for preparing cis-2,6-dimethylpiperazine |
US6365741B2 (en) | 1999-02-24 | 2002-04-02 | Bayer Aktiengesellschaft | Process for preparing Cis-2,6-dimethylpiperazine |
EP1284262A1 (en) * | 1999-02-24 | 2003-02-19 | Bayer Ag | Process for the preparation of cis-2,6-dimethylpiperazine |
Also Published As
Publication number | Publication date |
---|---|
FR1206423A (en) | 1960-02-09 |
DE1140939B (en) | 1962-12-13 |
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