GB650909A - Improvements in or relating to the preparation of diallyl ether dioxide - Google Patents
Improvements in or relating to the preparation of diallyl ether dioxideInfo
- Publication number
- GB650909A GB650909A GB20338/48A GB2033848A GB650909A GB 650909 A GB650909 A GB 650909A GB 20338/48 A GB20338/48 A GB 20338/48A GB 2033848 A GB2033848 A GB 2033848A GB 650909 A GB650909 A GB 650909A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diallyl ether
- dioxide
- monochlorhydrin
- epichlorhydrin
- solvent
- 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
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/28—Ethers with hydroxy compounds containing oxirane rings
Abstract
Diallyl ether dioxide is produced by dehydrohalogenating a diallyl ether dichlorhydrin in presence of an aqueous solution of p a strong base, preferably at 0-25 DEG C. The reaction mixture is extracted with a solvent such as carbon tetrachloride and the extract, after removal of solvent, distilled under reduced pressure. Hydroxides and carbonates of alkali or alkaline earth metals are suitable bases. In examples, diallyl ether dichlorhydrins are prepared by reacting the monochlorhydrin, obtained from epichlorhydrin and allyl alcohol, with hypochlorous acid, by reacting diallyl ether with hypochlorous acid or by treating glycerol b -monochlorhydrin with epichlorhydrin in presence of boron trifluoride in acetic acid at 100 DEG C. They are treated with aqueous caustic soda at 15 DEG C. or room temperature to yield the dioxide.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA650909X | 1947-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB650909A true GB650909A (en) | 1951-03-07 |
Family
ID=4172070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB20338/48A Expired GB650909A (en) | 1947-08-08 | 1948-07-30 | Improvements in or relating to the preparation of diallyl ether dioxide |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB650909A (en) |
-
1948
- 1948-07-30 GB GB20338/48A patent/GB650909A/en not_active Expired
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