GB345517A - A process for preparing cineol-containing oil mixtures - Google Patents
A process for preparing cineol-containing oil mixturesInfo
- Publication number
- GB345517A GB345517A GB10889/30A GB1088930A GB345517A GB 345517 A GB345517 A GB 345517A GB 10889/30 A GB10889/30 A GB 10889/30A GB 1088930 A GB1088930 A GB 1088930A GB 345517 A GB345517 A GB 345517A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cineol
- per cent
- product
- terpin
- acid
- 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
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic
- C07C35/08—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a six-membered rings
- C07C35/12—Menthol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Oil mixtures containing 1 : 8-cineol (eucalyptol), together with 1 : 4-cineol and terpene hydrocarbons, are obtained by the action of agents of the type commonly employed in the interconversion of terpene compounds (such as aqueous solutions of sulphuric acid, phosphoric acid, hydroxylated acids, sulphonic acids or bisulphates) on compounds of the same molecular formula as cineol or of a molecular formula differing from that of cineol by the addition of the elements of one or more molecules of water (e.g. terpin hydrate, terpin, terpineol, terpinenol), or on terpene hydrocarbons (such as pinene or sabinene) which on treatment with dilute acids are converted into initial materials of the above type, at temperatures below 80 DEG C., with immediate removal of the reaction product from the sphere of action. The temperature is kept lower, the higher the concentration of the acid or other agent employed. The removal of the product may be carried out by vacuum distillation or by extraction with indifferent solvents such as chloroform or toluene. In examples : (1) terpineol is treated with 30-40 per cent sulphuric or phosphoric acid at about 35 DEG C., the product, consisting of 22 per cent each of 1 ; 8- and 1 : 4-cineol and 45 per cent of hydrocarbons (limonene, terpinolene, a -, b - and d -terpinene), being continuously removed by vacuum distillation; (2) terpin is treated with 60 per cent sulphuric acid at -10 DEG C., and the product, of the same composition as in (1), is extracted by a stream of toluene, the extract being fractionally distilled. Specification 317,757, [Class 2 (iii), Dyes &c.], is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE345517X | 1929-04-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB345517A true GB345517A (en) | 1931-03-26 |
Family
ID=6254653
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10889/30A Expired GB345517A (en) | 1929-04-15 | 1930-04-05 | A process for preparing cineol-containing oil mixtures |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB345517A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4831163A (en) * | 1987-07-24 | 1989-05-16 | Union Camp Corporation | Improved method for the preparation of 1,4-cineole |
-
1930
- 1930-04-05 GB GB10889/30A patent/GB345517A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4831163A (en) * | 1987-07-24 | 1989-05-16 | Union Camp Corporation | Improved method for the preparation of 1,4-cineole |
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