GB458597A - Improvements in the manufacture of derivatives of polyhydroxy compounds - Google Patents
Improvements in the manufacture of derivatives of polyhydroxy compoundsInfo
- Publication number
- GB458597A GB458597A GB1798035A GB1798035A GB458597A GB 458597 A GB458597 A GB 458597A GB 1798035 A GB1798035 A GB 1798035A GB 1798035 A GB1798035 A GB 1798035A GB 458597 A GB458597 A GB 458597A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethyl
- cellulose
- etherification
- pyridine
- organic bases
- 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
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
Fibrous cellulosic materials are etherified under substantially anhydrous conditions in the presence of organic bases, by means of compounds of the general formula RX or R2SO4 as the sole etherifying agents, where X is a halogen atom and R is an alkyl or aralkyl hydrocarbon radicle or a carboxy or esterified carboxy substitution derivative thereof. Suitable etherifying agents are dimethyl and diethyl sulphates, methyl and ethyl chlorides, benzyl chloride, chloracetic acid, bromacetic acid, ethyl chloracetate, and ethyl bromacetate. As organic bases, methylamine, ethylamine, pyridine, piperidine, aniline, and methyl anilines are particularly useful. The etherification is preferably carried out in the presence of a water-immiscible diluent. In an example, cellulose is soaked in diethylamine, pressed, and introduced into an autoclave together with benzene and diethyl sulphate. In a second example, cellulose is treated in an autoclave with ethyl chloride in the presence of pyridine and ether. The products are suitable for conversion to other derivatives of cellulose, as is described in Specification 458,596. According to the Provisional Specification, the process is applicable to the etherification of other polymeric hydroxy compounds, e.g. polymerized vinyl alcohol and starch. Specifications 207,562, 249,173, 263,938, [all in Class 2 (ii)], and 414,751, [Group VIII], also are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1798035A GB458597A (en) | 1935-06-22 | 1935-06-22 | Improvements in the manufacture of derivatives of polyhydroxy compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1798035A GB458597A (en) | 1935-06-22 | 1935-06-22 | Improvements in the manufacture of derivatives of polyhydroxy compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB458597A true GB458597A (en) | 1936-12-22 |
Family
ID=10104561
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1798035A Expired GB458597A (en) | 1935-06-22 | 1935-06-22 | Improvements in the manufacture of derivatives of polyhydroxy compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB458597A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2476331A (en) * | 1945-11-15 | 1949-07-19 | Dow Chemical Co | Method of making methyl carboxymethyl cellulose |
US2618635A (en) * | 1949-12-23 | 1952-11-18 | Hercules Powder Co Ltd | Mixed cellulose ether |
-
1935
- 1935-06-22 GB GB1798035A patent/GB458597A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2476331A (en) * | 1945-11-15 | 1949-07-19 | Dow Chemical Co | Method of making methyl carboxymethyl cellulose |
US2618635A (en) * | 1949-12-23 | 1952-11-18 | Hercules Powder Co Ltd | Mixed cellulose ether |
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