GB1082118A - Quaternary ammonium halides - Google Patents
Quaternary ammonium halidesInfo
- Publication number
- GB1082118A GB1082118A GB3784164A GB3784164A GB1082118A GB 1082118 A GB1082118 A GB 1082118A GB 3784164 A GB3784164 A GB 3784164A GB 3784164 A GB3784164 A GB 3784164A GB 1082118 A GB1082118 A GB 1082118A
- Authority
- GB
- United Kingdom
- Prior art keywords
- product
- ammonium halides
- layer containing
- trimethyl ammonium
- quaternary ammonium
- 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
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/06—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms
- C07C209/12—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms with formation of quaternary ammonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Halo-ethyl trimethyl ammonium halides are made by reacting a 1,2-dihaloethane with trimethylamine in the presence of an amount of water and at a temperature and pressure sufficient to form a homogeneous solution with at least part of the reactants in the absence of product, and sufficient to dissolve the product to form an aqueous layer containing the product and a separate layer containing a substantial portion of any unreacted starting material. Preferred reaction temperatures are 100-150 DEG C. If the reactant is 1,2-dichloroethane, 20-30% by weight water, based on organic reactants, is employed. Examples relate to the preparation of 2-chloroethyl trimethyl ammonium chloride.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3900164 | 1964-09-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1082118A true GB1082118A (en) | 1967-09-06 |
Family
ID=10407000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3784164A Expired GB1082118A (en) | 1964-09-22 | 1964-09-16 | Quaternary ammonium halides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1082118A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0791575A1 (en) * | 1996-02-16 | 1997-08-27 | Nippon Paint Co., Ltd. | Method of synthesis of a quaternary ammonium salt |
-
1964
- 1964-09-16 GB GB3784164A patent/GB1082118A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0791575A1 (en) * | 1996-02-16 | 1997-08-27 | Nippon Paint Co., Ltd. | Method of synthesis of a quaternary ammonium salt |
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