GB496801A - Process for the manufacture of ethers of 2-methyl-2-hydroxy-3-chloro-tetrahydrofurane - Google Patents
Process for the manufacture of ethers of 2-methyl-2-hydroxy-3-chloro-tetrahydrofuraneInfo
- Publication number
- GB496801A GB496801A GB14292/38A GB1429238A GB496801A GB 496801 A GB496801 A GB 496801A GB 14292/38 A GB14292/38 A GB 14292/38A GB 1429238 A GB1429238 A GB 1429238A GB 496801 A GB496801 A GB 496801A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- hydroxy
- ethers
- tetrahydrofurane
- chloro
- 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
- C07D307/18—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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/20—Oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Alkyl ethers of 2-methyl-2-hydroxy-3-chlorotetrahydrofurane are prepared by treating a -aceto-a -chlorobutyrolactone with sulphuric acid and a primary aliphatic alcohol at a moderate temperature, preferably at 40-50 DEG C. Examples are given in which the methyl, ethyl and butyl ethers of 2-methyl-2-hydroxy-3-chlorotetrahydrofurane are prepared by treating a -aceto-a -chlorobutyrolactone with sulphuric acid and methanol, ethanol and n-butanol, respectively.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH496801X | 1937-07-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB496801A true GB496801A (en) | 1938-12-06 |
Family
ID=4516770
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14292/38A Expired GB496801A (en) | 1937-07-20 | 1938-05-13 | Process for the manufacture of ethers of 2-methyl-2-hydroxy-3-chloro-tetrahydrofurane |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB496801A (en) |
-
1938
- 1938-05-13 GB GB14292/38A patent/GB496801A/en not_active Expired
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