GB868421A - Improvements in or relating to trimethylolalkane products - Google Patents
Improvements in or relating to trimethylolalkane productsInfo
- Publication number
- GB868421A GB868421A GB32752/58A GB3275258A GB868421A GB 868421 A GB868421 A GB 868421A GB 32752/58 A GB32752/58 A GB 32752/58A GB 3275258 A GB3275258 A GB 3275258A GB 868421 A GB868421 A GB 868421A
- Authority
- GB
- United Kingdom
- Prior art keywords
- solution
- reaction
- trimethylolalkane
- water
- aqueous
- 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
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/18—Polyhydroxylic acyclic alcohols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Trimethylolalkanes are recovered from aqueous reaction liquors resulting from the reaction of formaldehyde with an aliphatic aldehyde containing from 3 to 5 carbon atoms in the presence of an alkali, by extracting the reaction liquor with a water-immiscible solvent to form a solvent solution of the extracted material, separating the solvent solution from the reaction liquor, contacting the separated solution with water to form an aqueous solution of the extracted material and separating the solvent, contacting the aqueous solution with a cation-exchange material and an anion exchange material, and evaporating the effluent from the ion exchange treatment to recover a trimethylolalkane. Suitable solvents are, for example, alcohols having 4-7 carbon atoms, particularly amyl alcohol, and ethyl acetate. It is desirable before extracting the reaction liquor to concentrate it by evaporating some of the water. Preferably the extraction is carried out at a temperature between 60 DEG and 90 DEG C. In a preferred method of carrying out the process the separated solution is steamdistilled to form the aqueous solution of the extracted material but, alternatively, the separated solution may be contacted with water and the aqueous phase separated, for example, by decantation. The aqueous reaction liquors used as starting materials may contain, in addition to the desired trimethylolalkane and the alkali metal formate, the following compounds:- <FORM:0868421/IV (b)/1> trimethylolkane, <FORM:0868421/IV (b)/2> monocyclic formal of trimethylolalkane, <FORM:0868421/IV (b)/3> linear formal or trimethylolakkane, and <FORM:0868421/IV (b)/4> in which R is an alkyl radical having 1-3 carbon atoms.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US868421XA | 1957-10-15 | 1957-10-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB868421A true GB868421A (en) | 1961-05-17 |
Family
ID=22201260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32752/58A Expired GB868421A (en) | 1957-10-15 | 1958-10-14 | Improvements in or relating to trimethylolalkane products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB868421A (en) |
-
1958
- 1958-10-14 GB GB32752/58A patent/GB868421A/en not_active Expired
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