GB1205618A - Enolic ethers of adipic dialdehydes and process for their preparation - Google Patents
Enolic ethers of adipic dialdehydes and process for their preparationInfo
- Publication number
- GB1205618A GB1205618A GB7791/68A GB779168A GB1205618A GB 1205618 A GB1205618 A GB 1205618A GB 7791/68 A GB7791/68 A GB 7791/68A GB 779168 A GB779168 A GB 779168A GB 1205618 A GB1205618 A GB 1205618A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dialdehydes
- adipic
- enolic
- inert
- vapours
- 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
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/277—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing ether groups, groups, groups, or groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/512—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being a free hydroxyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paper (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
1,205,618. Enolic ethers of adipic dialdehydes. UGINE KUHLMANN. 16 Feb., 1968 [9 March, 1967], No. 7791/68. Heading C2C. New enolic mono- and diethers of adipic dialdehydes of the general formulµ wherein R is the same or different and represents hydrogen, C 1-4 alkyl or optionally substituted phenyl and R<SP>1</SP> represents C 1-4 alkyl optionally substituted by halogen, hydroxy or nitrile, are prepared by heating a mono- or diether of 1,5-hexadiene-3,4-diol of formulae or their mixtures, to high temperatures to realise a Cope transposition. The process may be performed in the liquid phase in an inert, thermally stable solvent such as an aliphatic or aromatic hydrocarbon or an ether such as diphenylether, at atmospheric pressure and at the boiling point of the mixture. 0À01-1% of a polymerization inhibitor may be included, e.g. hydroquinone, monomethyl ether of hydroquinone, t-butyl-catechol, p-phenylene diamine or a copper salt. The heating time for the process may be 1/3-5 hours. The process may also be performed in the gaseous phase by passing the vapours of the starting material diluted if desired in an inert gas such as nitrogen, argon or CO 2 , into a duct which may contain matter inert to the vapours. These novel compounds may be used to generate the corresponding adipic dialdehydes since they are easily hydrolysed in a slightly acidic medium and thus may be made as disinfectants for water, textiles as bactericides, as reticulating and insolubilizing agents for proteins or polyhydroxylated polymers, in textile stiffening, paper treatment, reticulation of polyvinylic alcohols or other hydroxylated polymers. Also they may be used as monomers to carry out polymerization or copolymerization reactions with other vinylic monomers and are raw materials for the preparation of many di- or polyfunctional compounds such as 1,6-hexanediols and 1,6- diaminohexanes.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR98175A FR1523266A (en) | 1967-03-09 | 1967-03-09 | enolic ethers derived from adipic dialdehydes and method of preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1205618A true GB1205618A (en) | 1970-09-16 |
Family
ID=8626665
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7791/68A Expired GB1205618A (en) | 1967-03-09 | 1968-02-16 | Enolic ethers of adipic dialdehydes and process for their preparation |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS4936207B1 (en) |
BE (1) | BE709600A (en) |
CH (1) | CH493450A (en) |
FR (1) | FR1523266A (en) |
GB (1) | GB1205618A (en) |
LU (1) | LU55450A1 (en) |
NL (1) | NL6801858A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3714265A (en) * | 1970-01-09 | 1973-01-30 | A Bader | Hydroxy alkylene ethers of divinyl glycol |
USRE28387E (en) * | 1966-12-01 | 1975-04-08 | Hydroxy alkylene ethers of divinyl glycol | |
US3944591A (en) * | 1968-03-11 | 1976-03-16 | Andre Bader | Enolic ethers of adipic dialdehyde and method for preparing the same |
-
1967
- 1967-03-09 FR FR98175A patent/FR1523266A/en not_active Expired
-
1968
- 1968-01-19 BE BE709600D patent/BE709600A/xx unknown
- 1968-02-09 NL NL6801858A patent/NL6801858A/xx unknown
- 1968-02-09 LU LU55450D patent/LU55450A1/xx unknown
- 1968-02-16 GB GB7791/68A patent/GB1205618A/en not_active Expired
- 1968-03-08 CH CH344868A patent/CH493450A/en not_active IP Right Cessation
- 1968-03-09 JP JP43015185A patent/JPS4936207B1/ja active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
USRE28387E (en) * | 1966-12-01 | 1975-04-08 | Hydroxy alkylene ethers of divinyl glycol | |
US3944591A (en) * | 1968-03-11 | 1976-03-16 | Andre Bader | Enolic ethers of adipic dialdehyde and method for preparing the same |
US3714265A (en) * | 1970-01-09 | 1973-01-30 | A Bader | Hydroxy alkylene ethers of divinyl glycol |
Also Published As
Publication number | Publication date |
---|---|
JPS4936207B1 (en) | 1974-09-28 |
DE1668814A1 (en) | 1972-03-09 |
FR1523266A (en) | 1968-05-03 |
CH493450A (en) | 1970-07-15 |
NL6801858A (en) | 1968-09-10 |
BE709600A (en) | 1968-05-30 |
LU55450A1 (en) | 1968-04-23 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |