GB653653A - Improvements in and relating to the production of tetrahydrofurfuryl alcohol - Google Patents
Improvements in and relating to the production of tetrahydrofurfuryl alcoholInfo
- Publication number
- GB653653A GB653653A GB796148A GB796148A GB653653A GB 653653 A GB653653 A GB 653653A GB 796148 A GB796148 A GB 796148A GB 796148 A GB796148 A GB 796148A GB 653653 A GB653653 A GB 653653A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tetrahydrofurfuryl alcohol
- bisulphate
- alcohol
- furfural
- relating
- 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
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/12—Radicals substituted by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
Abstract
Tetrahydrofurfuryl alcohol is substantially freed from furfural and/or furfuryl alcohol by heating it with the bisulphate of an alkali metal, ammonia, or an alkaline earth metal or a mixture of such bisulphates, neutralizing the reaction mixture, and distilling off the tetrahydrofurfuryl alcohol; the bisulphate is used in an amount equal to or less than the amount that will dissolve in the tetrahydrofurfuryl alcohol at room temperature. The bisulphate may be added as a solid, preferably just sufficient to saturate the solution, e.g. 0.5 per cent, or as an aqueous solution, or it may be formed in situ from sodium sulphate and sulphuric acid. In an example, tetrahydrofurfuryl alcohol containing furfural, furfuryl alcohol, and water is purified by refluxing with varying amounts of sodium bisulphate; 15 minutes is the optimum time. Specifications 547,334 and 608,565 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB796148A GB653653A (en) | 1948-03-17 | 1948-03-17 | Improvements in and relating to the production of tetrahydrofurfuryl alcohol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB796148A GB653653A (en) | 1948-03-17 | 1948-03-17 | Improvements in and relating to the production of tetrahydrofurfuryl alcohol |
Publications (1)
Publication Number | Publication Date |
---|---|
GB653653A true GB653653A (en) | 1951-05-23 |
Family
ID=9843104
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB796148A Expired GB653653A (en) | 1948-03-17 | 1948-03-17 | Improvements in and relating to the production of tetrahydrofurfuryl alcohol |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB653653A (en) |
-
1948
- 1948-03-17 GB GB796148A patent/GB653653A/en not_active Expired
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