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GB760215A - Manufacture of alkanolamines - Google Patents

Manufacture of alkanolamines

Info

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
Application number
GB20498/51A
Inventor
Arnold John Lowe
Donald BUTLER
Edwin Marshall Meade
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Oxirane Ltd
Original Assignee
Oxirane Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Oxirane Ltd filed Critical Oxirane Ltd
Priority to GB20498/51A priority Critical patent/GB760215A/en
Publication of GB760215A publication Critical patent/GB760215A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C213/04Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C213/02Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/02Compounds 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
    • C07C215/04Compounds 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
    • C07C215/06Compounds 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
    • C07C215/08Compounds 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.
GB20498/51A 1951-08-30 1951-08-30 Manufacture of alkanolamines Expired GB760215A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (18)

* Cited by examiner, † Cited by third party
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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