GB1081355A - Production of tetrahydrodicyclopentadienylene diamine - Google Patents
Production of tetrahydrodicyclopentadienylene diamineInfo
- Publication number
- GB1081355A GB1081355A GB5151964A GB5151964A GB1081355A GB 1081355 A GB1081355 A GB 1081355A GB 5151964 A GB5151964 A GB 5151964A GB 5151964 A GB5151964 A GB 5151964A GB 1081355 A GB1081355 A GB 1081355A
- Authority
- GB
- United Kingdom
- Prior art keywords
- stage
- sulphuric acid
- diamine
- production
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/5026—Amines cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3234—Polyamines cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Tetrahydrodicyclopentadienylene diamine is prepared by reacting dicyclopentadiene with hydrocyanic acid and sulphuric acid in two stages, the first stage being carried out at - 5 DEG to + 20 DEG C. using 1 to 3 moles of sulphuric acid, while the second stage is carried out at a temperature of 0 DEG to 30 DEG C., such an amount of sulphuric acid being added that the total amount of sulphuric acid used is from 3 to 6 moles per mole of dicyclopentadiene, but at least one mole more than in the first stage, the reaction mixture then being hydrolysed and the diamine product being recovered by conventional methods. The whole of the hydrocyanic acid may be present in the first stage. Both the temperature and the strength of the sulphuric acid in the first stage are preferably lower than those in the second stage.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB74749A DE1227892B (en) | 1963-12-20 | 1963-12-20 | Process for the preparation of tetrahydrodicyclopentadienylenediamine |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1081355A true GB1081355A (en) | 1967-08-31 |
Family
ID=6978379
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5151964A Expired GB1081355A (en) | 1963-12-20 | 1965-12-18 | Production of tetrahydrodicyclopentadienylene diamine |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE657337A (en) |
DE (1) | DE1227892B (en) |
GB (1) | GB1081355A (en) |
LU (1) | LU47521A1 (en) |
NL (1) | NL6414662A (en) |
-
1963
- 1963-12-20 DE DEB74749A patent/DE1227892B/en active Pending
-
1964
- 1964-12-04 LU LU47521A patent/LU47521A1/xx unknown
- 1964-12-16 NL NL6414662A patent/NL6414662A/xx unknown
- 1964-12-18 BE BE657337D patent/BE657337A/xx unknown
-
1965
- 1965-12-18 GB GB5151964A patent/GB1081355A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
LU47521A1 (en) | 1965-02-04 |
DE1227892B (en) | 1966-11-03 |
NL6414662A (en) | 1965-06-21 |
BE657337A (en) | 1965-06-18 |
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