GB940252A - The process of manufacturing oxidation derivatives of decahydronaphthalene - Google Patents
The process of manufacturing oxidation derivatives of decahydronaphthaleneInfo
- Publication number
- GB940252A GB940252A GB19669/61A GB1966961A GB940252A GB 940252 A GB940252 A GB 940252A GB 19669/61 A GB19669/61 A GB 19669/61A GB 1966961 A GB1966961 A GB 1966961A GB 940252 A GB940252 A GB 940252A
- Authority
- GB
- United Kingdom
- Prior art keywords
- decahydronaphthalene
- cis
- pure
- ketones
- trans
- 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
- C07C409/00—Peroxy compounds
- C07C409/16—Peroxy compounds the —O—O— group being bound between two carbon atoms not further substituted by oxygen atoms, i.e. peroxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
- C07C407/003—Separation; Purification; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/02—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides
- C07C409/14—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides the carbon atom belonging to a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/14—All rings being cycloaliphatic
- C07C2602/26—All rings being cycloaliphatic the ring system containing ten carbon atoms
- C07C2602/28—Hydrogenated naphthalenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Trans-9-decahydronaphthalene peroxide and cis-a - and cis-b -decahydronaphthalene ketones and alcohols are produced by reacting pure decahydronaphthalene (as defined) with O2 or an O2-containing gas at 80 to 170 DEG C. "Pure decahydronaphthalene" is defined as decahydronaphthalene, consisting of at least 90% of cisdecahydronaphthalene, from which other substances contained in technically pure decahydronaphthalene have been removed. When the process is carried out at 80 to 110 DEG C. for 24 to 72 hours, the conversion kept below 30%, and water produced by secondary reactions immediately removed from the reaction zone, a product rich in trans-9-decahydronaphthalene peroxide is formed. When the process is carried out at 130 DEG to 170 DEG C. for 4 to 24 hours, the main reaction products are cis-a - and cis-b - decahydronaphthalene ketones and alcohols.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH811360A CH392494A (en) | 1960-07-16 | 1960-07-16 | Process for the preparation of a mixture containing trans-9-decahydronaphthalene hydroperoxide, cis-a- and cis-B-decalydronaphthol and cis-a- and cis-B-decahydronaphthalene ketone |
Publications (1)
Publication Number | Publication Date |
---|---|
GB940252A true GB940252A (en) | 1963-10-30 |
Family
ID=4335366
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19669/61A Expired GB940252A (en) | 1960-07-16 | 1961-05-31 | The process of manufacturing oxidation derivatives of decahydronaphthalene |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE605718A (en) |
CH (1) | CH392494A (en) |
DK (1) | DK120187B (en) |
ES (1) | ES267037A1 (en) |
GB (1) | GB940252A (en) |
-
1960
- 1960-07-16 CH CH811360A patent/CH392494A/en unknown
-
1961
- 1961-04-29 ES ES0267037A patent/ES267037A1/en not_active Expired
- 1961-05-06 DK DK187761AA patent/DK120187B/en unknown
- 1961-05-31 GB GB19669/61A patent/GB940252A/en not_active Expired
- 1961-07-04 BE BE605718A patent/BE605718A/en unknown
Also Published As
Publication number | Publication date |
---|---|
BE605718A (en) | 1961-11-03 |
ES267037A1 (en) | 1961-11-01 |
DK120187B (en) | 1971-04-26 |
CH392494A (en) | 1965-05-31 |
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