GB886367A - Improvements in and relating to hydrogenated binaphthyls and their preparation - Google Patents
Improvements in and relating to hydrogenated binaphthyls and their preparationInfo
- Publication number
- GB886367A GB886367A GB19531/60A GB1953160A GB886367A GB 886367 A GB886367 A GB 886367A GB 19531/60 A GB19531/60 A GB 19531/60A GB 1953160 A GB1953160 A GB 1953160A GB 886367 A GB886367 A GB 886367A
- Authority
- GB
- United Kingdom
- Prior art keywords
- potassium
- binaphthyl
- naphthalene
- sodium
- added
- 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
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/47—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with a bicyclo ring system containing ten carbon atoms
- C07C13/48—Completely or partially hydrogenated naphthalenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/74—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition with simultaneous hydrogenation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/01—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/02—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the alkali- or alkaline earth metals or beryllium
- C07C2523/04—Alkali metals
-
- 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
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The new compounds 1,2,3,4-tetrahydro-2,21-binaphthyl and 1,11,2,21,3,31,4,41-octahydro-2 21-binaphthyl are used as plasticizers for polyvinyl chloride or copolymers of vinyl chloride and vinyl acetate or as plasticizer extenders with dioctyl phthalate. In an example octahydrobinaphthyl is used in amounts of 41-51% by weight with 58,5-48,5% of a 97,5:2,5 vinyl chloride-vinyl acetate copolymer and 0,5% of dibutyltin maleate heat stabilizer.ALSO:The Specification comprises 1,2,3,4-tetrahydro-2,21-binaphthyl and 1,11,2,21,3,31,4,41-octahydro-2, 21-binaphthyl and their preparation by hydrogenating naphthalene at 150 DEG C.-300 DEG C. and a hydrogen pressure of 500-3,000 p.s.i.g. in the presence of at least 0.03% by weight based on the naphthalene of metallic potassium. The potassium may be added as such or formed in situ from sodium and a potassium compound which with the sodium liberates potassium, e.g. the oxide, hydroxide or sulphate. The preferred amount of potassium is 0.5%-3%. Sodium is preferably added in excess when a potassium compound is used or in addition when the metal is used by an amount of 1%-3% of the naphthalene. Tetralin in an amount equal in weight to the naphthalene may be added as solvent. The hydrogenated binaphthyls are recovered by distillation.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB19531/60A GB886367A (en) | 1960-06-02 | 1960-06-02 | Improvements in and relating to hydrogenated binaphthyls and their preparation |
FR830373A FR1259937A (en) | 1960-06-02 | 1960-06-17 | Process for the production of hydrogenated binaphthyls |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB19531/60A GB886367A (en) | 1960-06-02 | 1960-06-02 | Improvements in and relating to hydrogenated binaphthyls and their preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
GB886367A true GB886367A (en) | 1962-01-03 |
Family
ID=10130935
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19531/60A Expired GB886367A (en) | 1960-06-02 | 1960-06-02 | Improvements in and relating to hydrogenated binaphthyls and their preparation |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB886367A (en) |
-
1960
- 1960-06-02 GB GB19531/60A patent/GB886367A/en not_active Expired
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