GB573752A - Improvements in or relating to the production of condensation products of acetylene - Google Patents
Improvements in or relating to the production of condensation products of acetyleneInfo
- Publication number
- GB573752A GB573752A GB1530741A GB1530741A GB573752A GB 573752 A GB573752 A GB 573752A GB 1530741 A GB1530741 A GB 1530741A GB 1530741 A GB1530741 A GB 1530741A GB 573752 A GB573752 A GB 573752A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acetylene
- reaction products
- compounds
- nitroaryl
- radicle
- 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
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/60—Preparation of compounds containing amino groups bound to a carbon skeleton by condensation or addition reactions, e.g. Mannich reaction, addition of ammonia or amines to alkenes or to alkynes or addition of compounds containing an active hydrogen atom to Schiff's bases, quinone imines, or aziranes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
Polymerizable N - vinyl compounds are obtained by condensing acetylene with a body of the formula R-NH-X where R is an alkyl, aryl, acyl, aracyl or an ester radicle and X is a chlorine, bromine, iodine, nitrile, nitro, nitroaryl, or sulphonic radicle having in aqueous solution a pH less than 7. Suitable compounds are N-chloracrylamides, N-cyanacrylamides, N-nitroacrylamides, N-chlorurethanes, N-cyanurethanes, N-nitrourethanes, N-acylsulphonamides, N-alkyl- or N-aryl-nitramines and N-(nitroaryl)amines. Suitable condensing agents are preferably used such as mercuric salts, cadmium and zinc compounds and heteropolyacids; the agent may be produced in situ for instance by adding sulphuric acid to a reaction mixture containing a dissolved or suspended mercury salt. The reaction may be effected in the presence or absence of solvents, such as ketones, ethylidene diacetate and other inert oxygen-containing solvents, or the liquid reaction products remaining in the residue after the lower-boiling unsaturated reaction products have been removed by distillation. A polymerization inhibitor such as copper or a phenol may be present. Instead of employing distillation, unchanged starting material may be removed from the reaction products by aqueous alkali. In an example acetylene is introduced into a mixture of monochlorurethane, mercuric acetate, and sulphuric acid at room temperature. Vinyl chlorurethane is distilled from the product. It polymerizes to a glass-clear product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1530741A GB573752A (en) | 1940-12-20 | 1940-12-20 | Improvements in or relating to the production of condensation products of acetylene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1530741A GB573752A (en) | 1940-12-20 | 1940-12-20 | Improvements in or relating to the production of condensation products of acetylene |
Publications (1)
Publication Number | Publication Date |
---|---|
GB573752A true GB573752A (en) | 1945-12-05 |
Family
ID=10056759
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1530741A Expired GB573752A (en) | 1940-12-20 | 1940-12-20 | Improvements in or relating to the production of condensation products of acetylene |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB573752A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2772306A (en) * | 1954-05-10 | 1956-11-27 | George R Thomas | Process for the preparation of chloronitro-carbamic acid ester |
WO2006015799A1 (en) * | 2004-08-05 | 2006-02-16 | Basf Aktiengesellschaft | Stabilizers for use in nvp synthesis |
-
1940
- 1940-12-20 GB GB1530741A patent/GB573752A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2772306A (en) * | 1954-05-10 | 1956-11-27 | George R Thomas | Process for the preparation of chloronitro-carbamic acid ester |
WO2006015799A1 (en) * | 2004-08-05 | 2006-02-16 | Basf Aktiengesellschaft | Stabilizers for use in nvp synthesis |
JP2008508346A (en) * | 2004-08-05 | 2008-03-21 | ビーエーエスエフ ソシエタス・ヨーロピア | Stabilizer for NVP synthesis |
US7674934B2 (en) | 2004-08-05 | 2010-03-09 | Basf Aktiengesellschaft | Stabilizers for use in NVP synthesis |
CN101035757B (en) * | 2004-08-05 | 2011-06-01 | 巴斯福股份公司 | Stabilizers for use in NVP synthesis |
DE112005001915B4 (en) * | 2004-08-05 | 2017-03-02 | Basf Se | Stabilizers for NVP synthesis |
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