GB1014265A - Improvements in or relating to halohydrin ethers - Google Patents
Improvements in or relating to halohydrin ethersInfo
- Publication number
- GB1014265A GB1014265A GB4149864A GB4149864A GB1014265A GB 1014265 A GB1014265 A GB 1014265A GB 4149864 A GB4149864 A GB 4149864A GB 4149864 A GB4149864 A GB 4149864A GB 1014265 A GB1014265 A GB 1014265A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloropropane
- butoxy
- preferred
- relating
- alcohol
- 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
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/12—Saturated ethers containing halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises 1-t-butoxy-2-chloropropane, 2 - t - butoxy - 1 - chloropropane and the preparation of 1,2-halohydrin ethers by reacting an olefinic hydrocarbon with a mono- or di-hydric alcohol and either bromine or chlorine in the presence of an alkali metal bicarbonate. Preferred olefinic hydrocarbons are the alkenes of the general formula RCH: CHR1 where R and R1 represent alkyl radicals or hydrogen atoms. It is also preferred to employ an excess of both olefinic hydrocarbon and alcohol and to perform the reaction in the liquid phase. Reaction temperatures are generally from - 10 DEG C. to + 50 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4149864A GB1014265A (en) | 1964-10-12 | 1964-10-12 | Improvements in or relating to halohydrin ethers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4149864A GB1014265A (en) | 1964-10-12 | 1964-10-12 | Improvements in or relating to halohydrin ethers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1014265A true GB1014265A (en) | 1965-12-22 |
Family
ID=10419969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4149864A Expired GB1014265A (en) | 1964-10-12 | 1964-10-12 | Improvements in or relating to halohydrin ethers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1014265A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3444243A (en) * | 1965-01-13 | 1969-05-13 | Montedison Spa | Process for the preparation of beta-halogen ethers |
-
1964
- 1964-10-12 GB GB4149864A patent/GB1014265A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3444243A (en) * | 1965-01-13 | 1969-05-13 | Montedison Spa | Process for the preparation of beta-halogen ethers |
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