GB189816994A - Improvements in the Manufacture of Fine Chemical Products for Use in Pharmacy and other Purposes. - Google Patents
Improvements in the Manufacture of Fine Chemical Products for Use in Pharmacy and other Purposes.Info
- Publication number
- GB189816994A GB189816994A GB189816994DA GB189816994A GB 189816994 A GB189816994 A GB 189816994A GB 189816994D A GB189816994D A GB 189816994DA GB 189816994 A GB189816994 A GB 189816994A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- camphorate
- hydrogen
- sodium
- phenolic
- 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
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
16,994. Wellcome, H. S., and Schryver, S. B. Aug. 6. Medicinal preparations.-Acid phenolic salts of dibasic acids, for use in pharmacy, are produced by acting with a sodium phenol compound upon an anhydride of a dibasic acid in the presence of a chemically-inactive liquid, and then decomposing the sodium phenolic salt of the acid thus produced by a dilute mineral acid. In most cases it is convenient to mix the phenol with a solvent, such as xylene or benzene, to dissolve metallic sodium in the phenol solution, heat being applied if necessary, and then to add the anhydride to the solution. A gelatinous precipitate of the sodium phenolic salt separates, and this is usually washed out with water. The acid phenolic salt is precipitated from the washings by a mineral acid, and it is purified by recrystallization from a suitable solvent. When the sodium phenolic salt is very easily hydrolysed by water, it is separated from the solvent, pressed, dried, and powdered, and is then decomposed by a ten per cent. sulphuric-acid solution covered by ether, which will dissolve the liberated acid phenolic salt. The following acid salts are produced by the foregoing processes, viz. :-hydrogen thymol succinate, camphorate, and phthalate ; hydrogen guaiacol camphorate and succinate; hydrogen carvacrol camphorate ; hydrogen #-naphthol camphorate ; hydrogen salol camphorate; hydrogen p-bromophenol camphorate ; hydrogen 2 : 4 dibromophenol camphorate; and hydrogen m-nitrophenol camphorate. The acid phenolic salts may be converted into metallic, alkylic, and phenylic derivatives.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB189816994T | 1898-08-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB189816994A true GB189816994A (en) | 1899-07-15 |
Family
ID=32416937
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB189816994D Expired GB189816994A (en) | 1898-08-06 | 1898-08-06 | Improvements in the Manufacture of Fine Chemical Products for Use in Pharmacy and other Purposes. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB189816994A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2443473A (en) * | 1943-09-17 | 1948-06-15 | Research Corp | Phosphoric acid ester of vitamin a |
-
1898
- 1898-08-06 GB GB189816994D patent/GB189816994A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2443473A (en) * | 1943-09-17 | 1948-06-15 | Research Corp | Phosphoric acid ester of vitamin a |
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