GB741702A - Improvements in or relating to processes for producing trioxocane and tetroxocane products - Google Patents
Improvements in or relating to processes for producing trioxocane and tetroxocane productsInfo
- Publication number
- GB741702A GB741702A GB29915/53A GB2991553A GB741702A GB 741702 A GB741702 A GB 741702A GB 29915/53 A GB29915/53 A GB 29915/53A GB 2991553 A GB2991553 A GB 2991553A GB 741702 A GB741702 A GB 741702A
- Authority
- GB
- United Kingdom
- Prior art keywords
- trioxocane
- give
- diethylene glycol
- react
- ethyl
- 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
- C07D323/00—Heterocyclic compounds containing more than two oxygen atoms as the only ring hetero atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Compounds of general formula <FORM:0741702/IV(a)/1> in which n is 2 or 3 and R is hydrogen or an aliphatic radical are prepared by a process comprising contacting a mixture of formaldehyde or an aliphatic aldehyde and diethylene glycol or triethylene glycol with an acidic cation exchange resin at elevated temperature. Suitable aldehydes are, for example, acetaldehyde, propionaldehyde isobutyraldehyde, 2 - ethyl butyraldehyde, chloral and dichloroacetaldehyde. Advantageously solvents, e.g. benzene, may be used for the reaction mixture. Suitable acidic cation exchange resins are, for example, sulphonated coal-type resins, sulphonated phenol-formaldehyde resins, and sulphonated polystyrene-type resins. In the examples (a) diethylene glycol and paraformaldehyde are reacted to give 1,3,6-trioxocane; (b) dichloroacetaldehyde and diethylene glycol react to give 2 - dichloromethyl - 1,3,6 - trioxocane; (c) diethylene glycol and paraformaldehyde react to give 1,3,6-trioxocane; (d) diethylene glycol and isobutyraldehyde react to give 2-isopropyl-1,3,6-trioxocane; (e) diethylene glycol and 2-ethyl-butyraldehyde react to give 1-ethyl-n-propyl-1,3,6-trioxocane; and (f) triethylene glycol and formaldehyde react to give 1,3,6,9-tetroxacyclohendecane; all the reactions taking place in the presence of an acidic cation exchange resin at elevated temperature.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US741702XA | 1952-10-30 | 1952-10-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB741702A true GB741702A (en) | 1955-12-07 |
Family
ID=22118108
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB29915/53A Expired GB741702A (en) | 1952-10-30 | 1953-10-29 | Improvements in or relating to processes for producing trioxocane and tetroxocane products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB741702A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3197420A (en) * | 1959-08-07 | 1965-07-27 | Hoechst Ag | Process for polymerizing 1, 3, 6-trioxacyclo-octanes |
-
1953
- 1953-10-29 GB GB29915/53A patent/GB741702A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3197420A (en) * | 1959-08-07 | 1965-07-27 | Hoechst Ag | Process for polymerizing 1, 3, 6-trioxacyclo-octanes |
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