GB760215A - Manufacture of alkanolamines - Google Patents
Manufacture of alkanolaminesInfo
- Publication number
- GB760215A GB760215A GB20498/51A GB2049851A GB760215A GB 760215 A GB760215 A GB 760215A GB 20498/51 A GB20498/51 A GB 20498/51A GB 2049851 A GB2049851 A GB 2049851A GB 760215 A GB760215 A GB 760215A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ammonia
- alkylene oxide
- water
- mono
- mixture
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/04—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reaction of ammonia or amines with olefin oxides or halohydrins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/08—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic with only one hydroxy group and one amino group bound to the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Alkanolamines are prepared from ammonia and ethylene oxide or 1 : 2-propylene oxide by continuously passing a liquid mixture of ammonia in aqueous solution, containing 5 to 90 per cent by weight of water, and the alkylene oxide, which mixture contains not more than 50 per cent by weight of the alkylene oxide and from 1 to 45 mols. of ammonia for every three mols. of alkylene oxide present, through a reaction zone maintained at a temperature ranging from a minimum of 80 DEG to 150 DEG C. to a maximum of 275 DEG C., under a pressure which ensures that the reaction mixture is maintained in the liquid state throughout the reaction zone, the contact time within the reaction zone not exceeding 30 minutes and the amount of water in the mixture and the temperature of the reaction zone being so adjusted in relation to each other that substantially complete reaction of the alkylene oxide takes place. In a modification, all or part of the water in the reaction mixture is replaced by an equivalent amount in terms of hydroxyl content of an organic compound containing only carbon, hydrogen and one or more alcoholic or phenolic hydroxy groups, e.g. methanol, ethanol, ethylene glycol, glycerol or phenol. Preferably, the reaction zone is first heated to 80-150 DEG C. and then cooled to maintain a temperature of about 150 DEG C. or lower. The proportions of mono-, di- and tri-alkanolamines in the product may be varied by adjustment of the ratio of ammonia to alkylene oxide. Thus, a ratio of ammonia to ethylene oxide of greater than 4 : 1 gives mono-ethanolamine predominantly; a ratio of 1 : 1 to 4 : 1 gives optimum proportions of diethanol amine; a ratio of 1 : 3 using very dilute aqueous ammonia favours triethanolamine formation. The products contain some tri-alkanolamine glycol ethers; formation of those derived from triethanolamine may be suppressed by including minor amounts of acidic materials such as sulphuric, phosphoric or boric acids or carbon dioxide in the reaction mixture. A preferred embodiment comprises the use of aqueous ammonia containing 40-80 per cent in a reaction mixture containing not more than 35 per cent by weight of alkylene oxide and heating to an initial temperature of 100-150 DEG C., which allows a contact time of 120 seconds or less to be used and yields predominantly mono-alkanol amines. The mono-and di-alkanolamines obtained by the present process may be further reacted with the alkylene oxides. Suitable apparatus is described comprising proportionating pumps which feed aqueous ammonia and alkylene oxide to a mixer from which the resulting mixture is fed through a long stainless steel coil completely immersed in a liquid, e.g. water, boiling under reflux. The boiling liquid heats the reactants to the boiling temperature and the exothermic heat of the subsequent reaction is consumed in further boiling the controlling liquid. The reacted mixture leaves the reactor, at a pressure of, e.g., 60 atmospheres, through a let-down valve, and is fractionated to separate the excess ammonia, water and alkanolamines. Numerous examples are given of process employing this apparatus wherein aqueous ammonia is reacted with ethylene or propylene oxide yielding mixtures of the corresponding three trialkanolamines, and in some cases the crude products containing aqueous excess ammonia or an isolated ethanolamine are further reacted with the alkylene oxide. Other examples describe similar reactions of ethylene oxide with ammonia in methanol, aqueous methanol or n-butanol. According to the Provisional Specification, the process may be carried out at temperatures as high as 300 DEG C.; the reaction mixture should contain more than 1 per cent by weight of water and the contact time should be such that complete reaction of the alkylene oxide occurs and may be 2 hours. Additional examples are given wherein a molar ratio of ammonia to ethylene oxide of 25 : 1 and a 95 per cent aqueous ammonia solution are used. Also, the organic compounds which may replace the water wholly or in part may be any hydroxy compound including mono-, di- or tri-alkanolamines produced by the process and examples are given wherein mixtures of ammonia with mono- or di-ethanolamine are reacted with ethylene oxide. Specifications 448,373, [Group IV], 642,950, 655,580 and U.S.A. Specification 2,373,199 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB20498/51A GB760215A (en) | 1951-08-30 | 1951-08-30 | Manufacture of alkanolamines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB20498/51A GB760215A (en) | 1951-08-30 | 1951-08-30 | Manufacture of alkanolamines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB760215A true GB760215A (en) | 1956-10-31 |
Family
ID=10146877
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB20498/51A Expired GB760215A (en) | 1951-08-30 | 1951-08-30 | Manufacture of alkanolamines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB760215A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3357132A (en) * | 1964-08-27 | 1967-12-12 | Olin Mathieson | Method of protecting plants in a salt-containing environment |
US3544632A (en) * | 1967-04-13 | 1970-12-01 | Basf Ag | Production of alkanolamines-(1,2) or cycloalkanolamines-(1,2) |
US4356323A (en) * | 1980-04-12 | 1982-10-26 | Axel Kleemann | Process for the production of 1-amino-propanediol-(2,3) (I) |
US4358615A (en) * | 1980-04-12 | 1982-11-09 | Degussa Aktiengesellschaft | Process for the production of 1-amino-propanediol-(2,3) (II) |
US4360697A (en) * | 1980-04-12 | 1982-11-23 | Degussa Aktiengesellschaft | Process for the production of 1-amino-propanediol-2,3 |
US6388137B1 (en) | 1998-12-01 | 2002-05-14 | Basf Aktiengesellschaft | Method of purifying triethanolamine |
US6469214B2 (en) | 2000-12-01 | 2002-10-22 | Basf Aktiengesellschaft | Process for the preparation of ethanolamines |
FR2851564A1 (en) * | 2003-02-24 | 2004-08-27 | Bp Lavera Snc | Combined process for the manufacture of ethylene oxide and ethanolamines, by catalytic oxidation of ethylene and subsequent reaction of part of the ethylene oxide produced with ammonia |
US6974883B2 (en) | 2000-01-24 | 2005-12-13 | Bp Chemicals Limited | Process for manufacturing triethanolamine and product obtained |
CN102659608A (en) * | 2012-04-28 | 2012-09-12 | 薛荔 | Method for preparing MNPA, DNPA and TNPA |
WO2015102985A1 (en) | 2013-12-30 | 2015-07-09 | Scientific Design Company, Inc. | Process for making ethanolamines |
WO2015102984A1 (en) | 2013-12-30 | 2015-07-09 | Scientific Design Company, Inc. | Process for making ethanolamines |
CN110981738A (en) * | 2019-12-30 | 2020-04-10 | 杭州新本立医药有限公司 | Synthesis method of 2-aminopropanol |
-
1951
- 1951-08-30 GB GB20498/51A patent/GB760215A/en not_active Expired
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3357132A (en) * | 1964-08-27 | 1967-12-12 | Olin Mathieson | Method of protecting plants in a salt-containing environment |
US3544632A (en) * | 1967-04-13 | 1970-12-01 | Basf Ag | Production of alkanolamines-(1,2) or cycloalkanolamines-(1,2) |
US4356323A (en) * | 1980-04-12 | 1982-10-26 | Axel Kleemann | Process for the production of 1-amino-propanediol-(2,3) (I) |
US4358615A (en) * | 1980-04-12 | 1982-11-09 | Degussa Aktiengesellschaft | Process for the production of 1-amino-propanediol-(2,3) (II) |
US4360697A (en) * | 1980-04-12 | 1982-11-23 | Degussa Aktiengesellschaft | Process for the production of 1-amino-propanediol-2,3 |
MY119691A (en) * | 1998-12-01 | 2005-06-30 | Basf Ag | Method of purifying triethanolamine |
US6388137B1 (en) | 1998-12-01 | 2002-05-14 | Basf Aktiengesellschaft | Method of purifying triethanolamine |
US6974883B2 (en) | 2000-01-24 | 2005-12-13 | Bp Chemicals Limited | Process for manufacturing triethanolamine and product obtained |
US6469214B2 (en) | 2000-12-01 | 2002-10-22 | Basf Aktiengesellschaft | Process for the preparation of ethanolamines |
FR2851564A1 (en) * | 2003-02-24 | 2004-08-27 | Bp Lavera Snc | Combined process for the manufacture of ethylene oxide and ethanolamines, by catalytic oxidation of ethylene and subsequent reaction of part of the ethylene oxide produced with ammonia |
CN102659608A (en) * | 2012-04-28 | 2012-09-12 | 薛荔 | Method for preparing MNPA, DNPA and TNPA |
CN102659608B (en) * | 2012-04-28 | 2016-02-24 | 薛荔 | Prepare the method for new Propanolamine |
WO2015102985A1 (en) | 2013-12-30 | 2015-07-09 | Scientific Design Company, Inc. | Process for making ethanolamines |
WO2015102984A1 (en) | 2013-12-30 | 2015-07-09 | Scientific Design Company, Inc. | Process for making ethanolamines |
US9120720B2 (en) | 2013-12-30 | 2015-09-01 | Scientific Design Company, Inc. | Process for making ethanolamines |
US9227912B2 (en) | 2013-12-30 | 2016-01-05 | Scientific Design Company, Inc. | Process for making ethanolamines |
CN110981738A (en) * | 2019-12-30 | 2020-04-10 | 杭州新本立医药有限公司 | Synthesis method of 2-aminopropanol |
CN110981738B (en) * | 2019-12-30 | 2022-09-20 | 杭州新本立医药有限公司 | Synthesis method of 2-aminopropanol |
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