GB704226A - Process for making polyalkanolamines - Google Patents
Process for making polyalkanolaminesInfo
- Publication number
- GB704226A GB704226A GB754852A GB754852A GB704226A GB 704226 A GB704226 A GB 704226A GB 754852 A GB754852 A GB 754852A GB 754852 A GB754852 A GB 754852A GB 704226 A GB704226 A GB 704226A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxide
- monoisopropanolamine
- diethanolamine
- reacted
- give
- 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
- 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
- C07C215/12—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 the nitrogen atom of the amino group being further bound to hydrocarbon groups substituted by hydroxy groups
Abstract
Polyalkanolamines are obtained by passing an olefine oxide containing not more than five carbon atoms into contact with an anhydrous alkanolamine of formula R-NH-R1, in which R is a monohydroxy alkyl radical and R1 is hydrogen or a monohydroxy alkyl radical, neither of which contains more than five carbon atoms, in the absence of a solvent and of ammonia, at a temperature maintained between 0 DEG and 100 DEG C., the oxide being added in a molecular proportion, relative to the alkanolamine, not exceeding 1:1 when R1 is a monohydroxy alkyl radical and not exceeding 2:1 when R1 is hydrogen. Suitable oxides are ethylene oxide, propylene oxide, isobutylene oxide and butadiene monoxide. Suitable alkanolamines as starting materials, are monoethanolamine, monoisopropanolamine, monoisobutanolamine, diethanolamine, diisopropanolamine and monoethanol monoisopropanolamine. Preferably the reaction is conducted under reflux or in a closed vessel at a pressure at least equal to the autogenous pressure of the reaction mixture. In the examples (a) monoethanolamine is reacted with ethylene oxide to give a mixture of triethanolamine and diethanolamine; (b) propylene oxide is reacted with monoisopropanolamine to give triisopropanolamine with a little di-isopropanolamine; and (c) propylene oxide is reacted with diethanolamine to give diethanolmonoisopropanolamine. U.S.A. Specification 2,373,199 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB754852A GB704226A (en) | 1952-03-24 | 1952-03-24 | Process for making polyalkanolamines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB754852A GB704226A (en) | 1952-03-24 | 1952-03-24 | Process for making polyalkanolamines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB704226A true GB704226A (en) | 1954-02-17 |
Family
ID=9835244
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB754852A Expired GB704226A (en) | 1952-03-24 | 1952-03-24 | Process for making polyalkanolamines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB704226A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3151166A (en) * | 1960-09-12 | 1964-09-29 | Jefferson Chem Co Inc | Method for preparing color stable ethanolamines |
CN102924301A (en) * | 2012-11-01 | 2013-02-13 | 史才军 | Preparation method of N,N-bis(2-hydroxyethyl)isopropanolamine |
CN103224453A (en) * | 2013-03-28 | 2013-07-31 | 宁波市联凯化学有限公司 | Method for preparing diethanol isopropanol amine |
CN106746845A (en) * | 2016-11-16 | 2017-05-31 | 宁波远利化工有限公司 | A kind of production technology of cement grinding aid |
-
1952
- 1952-03-24 GB GB754852A patent/GB704226A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3151166A (en) * | 1960-09-12 | 1964-09-29 | Jefferson Chem Co Inc | Method for preparing color stable ethanolamines |
CN102924301A (en) * | 2012-11-01 | 2013-02-13 | 史才军 | Preparation method of N,N-bis(2-hydroxyethyl)isopropanolamine |
CN102924301B (en) * | 2012-11-01 | 2014-04-02 | 史才军 | Preparation method of N,N-bis(2-hydroxyethyl)isopropanolamine |
CN103224453A (en) * | 2013-03-28 | 2013-07-31 | 宁波市联凯化学有限公司 | Method for preparing diethanol isopropanol amine |
CN106746845A (en) * | 2016-11-16 | 2017-05-31 | 宁波远利化工有限公司 | A kind of production technology of cement grinding aid |
CN106746845B (en) * | 2016-11-16 | 2018-10-02 | 宁波远利化工有限公司 | A kind of production technology of cement grinding aid |
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